Canonical Allele Identifier: CA2207327683
Gene: CIITA HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10908981_10908991delinsAGGTCTAGCCT , CM000678.2:g.10908981_10908991delinsAGGTCTAGCCT GRCh38
NC_000016.9:g.11002838_11002848delinsAGGTCTAGCCT , CM000678.1:g.11002838_11002848delinsAGGTCTAGCCT GRCh37
NC_000016.8:g.10910339_10910349delinsAGGTCTAGCCT NCBI36
NG_009628.1:g.36784_36794delinsAGGTCTAGCCT , LRG_49:g.36784_36794delinsAGGTCTAGCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000324288.14:c.2658-48_2658-38delinsAGGTCTAGCCT MANE Select ENSP00000316328.8:n.2658-48_2658-38delinsAGGTCTAGCCT
ENST00000324288.12:c.2658-48_2658-38delinsAGGTCTAGCCT ENSP00000316328.8:n.2658-48_2658-38delinsAGGTCTAGCCT
ENST00000381835.9:c.860-2_868delinsAGGTCTAGCCT
ENST00000537380.1:n.1007-1207_1007-1197delinsAGGTCTAGCCT
ENST00000570546.5:n.3610_3620delinsAGGTCTAGCCT
ENST00000618207.4:c.1007-1207_1007-1197delinsAGGTCTAGCCT ENSP00000484761.1:n.1007-1207_1007-1197delinsAGGTCTAGCCT
ENST00000618327.4:c.2661-48_2661-38delinsAGGTCTAGCCT ENSP00000485010.1:n.2661-48_2661-38delinsAGGTCTAGCCT
NM_000246.3:c.2658-48_2658-38delinsAGGTCTAGCCT , LRG_49t1:c.2658-48_2658-38delinsAGGTCTAGCCT NP_000237.2:n.2658-48_2658-38delinsAGGTCTAGCCT
NM_001286402.1:c.2661-48_2661-38delinsAGGTCTAGCCT NP_001273331.1:n.2661-48_2661-38delinsAGGTCTAGCCT
NM_001286403.1:c.860-2_868delinsAGGTCTAGCCT
NR_104444.1:n.1140-1207_1140-1197delinsAGGTCTAGCCT
XM_006720880.2:c.2955-48_2955-38delinsAGGTCTAGCCT XP_006720943.2:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522484.1:c.2955-48_2955-38delinsAGGTCTAGCCT XP_011520786.1:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522485.1:c.2955-48_2955-38delinsAGGTCTAGCCT XP_011520787.1:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522486.1:c.2955-48_2955-38delinsAGGTCTAGCCT XP_011520788.1:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522487.1:c.2709-48_2709-38delinsAGGTCTAGCCT XP_011520789.1:n.2709-48_2709-38delinsAGGTCTAGCCT
XM_011522488.1:c.2706-48_2706-38delinsAGGTCTAGCCT XP_011520790.1:n.2706-48_2706-38delinsAGGTCTAGCCT
XM_011522489.1:c.2706-48_2706-38delinsAGGTCTAGCCT XP_011520791.1:n.2706-48_2706-38delinsAGGTCTAGCCT
XM_011522490.1:c.2703-48_2703-38delinsAGGTCTAGCCT XP_011520792.1:n.2703-48_2703-38delinsAGGTCTAGCCT
XM_011522491.1:c.2955-48_2955-38delinsAGGTCTAGCCT XP_011520793.1:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522492.1:c.2661-48_2661-38delinsAGGTCTAGCCT XP_011520794.1:n.2661-48_2661-38delinsAGGTCTAGCCT
XM_011522493.1:c.2658-48_2658-38delinsAGGTCTAGCCT XP_011520795.1:n.2658-48_2658-38delinsAGGTCTAGCCT
XM_011522494.1:c.2589-48_2589-38delinsAGGTCTAGCCT XP_011520796.1:n.2589-48_2589-38delinsAGGTCTAGCCT
XM_011522495.1:c.2514-48_2514-38delinsAGGTCTAGCCT XP_011520797.1:n.2514-48_2514-38delinsAGGTCTAGCCT
XM_011522496.1:c.2511-48_2511-38delinsAGGTCTAGCCT XP_011520798.1:n.2511-48_2511-38delinsAGGTCTAGCCT
XR_932841.1:n.2970-48_2970-38delinsAGGTCTAGCCT
XR_932842.1:n.2970-48_2970-38delinsAGGTCTAGCCT
XR_932843.1:n.2970-48_2970-38delinsAGGTCTAGCCT
XR_932846.1:n.2970-2_2978delinsAGGTCTAGCCT
XR_932847.1:n.2970-2_2978delinsAGGTCTAGCCT
XR_932848.1:n.1010-2_1018delinsAGGTCTAGCCT
XM_006720880.3:c.2955-48_2955-38delinsAGGTCTAGCCT XP_006720943.2:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522484.3:c.2955-48_2955-38delinsAGGTCTAGCCT XP_011520786.1:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522485.2:c.2955-48_2955-38delinsAGGTCTAGCCT XP_011520787.1:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522486.2:c.2955-48_2955-38delinsAGGTCTAGCCT XP_011520788.1:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522487.2:c.2709-48_2709-38delinsAGGTCTAGCCT XP_011520789.1:n.2709-48_2709-38delinsAGGTCTAGCCT
XM_011522488.2:c.2706-48_2706-38delinsAGGTCTAGCCT XP_011520790.1:n.2706-48_2706-38delinsAGGTCTAGCCT
XM_011522489.2:c.2706-48_2706-38delinsAGGTCTAGCCT XP_011520791.1:n.2706-48_2706-38delinsAGGTCTAGCCT
XM_011522490.2:c.2703-48_2703-38delinsAGGTCTAGCCT XP_011520792.1:n.2703-48_2703-38delinsAGGTCTAGCCT
XM_011522491.2:c.2955-48_2955-38delinsAGGTCTAGCCT XP_011520793.1:n.2955-48_2955-38delinsAGGTCTAGCCT
XM_011522492.2:c.2661-48_2661-38delinsAGGTCTAGCCT XP_011520794.1:n.2661-48_2661-38delinsAGGTCTAGCCT
XM_011522493.2:c.2658-48_2658-38delinsAGGTCTAGCCT XP_011520795.1:n.2658-48_2658-38delinsAGGTCTAGCCT
XM_011522494.2:c.2589-48_2589-38delinsAGGTCTAGCCT XP_011520796.1:n.2589-48_2589-38delinsAGGTCTAGCCT
XM_011522495.2:c.2514-48_2514-38delinsAGGTCTAGCCT XP_011520797.1:n.2514-48_2514-38delinsAGGTCTAGCCT
XM_011522496.2:c.2511-48_2511-38delinsAGGTCTAGCCT XP_011520798.1:n.2511-48_2511-38delinsAGGTCTAGCCT
XM_024450280.1:c.2901-48_2901-38delinsAGGTCTAGCCT XP_024306048.1:n.2901-48_2901-38delinsAGGTCTAGCCT
XM_024450281.1:c.2754-48_2754-38delinsAGGTCTAGCCT XP_024306049.1:n.2754-48_2754-38delinsAGGTCTAGCCT
XR_001751904.1:n.2974-2_2982delinsAGGTCTAGCCT
XR_932841.3:n.2972-48_2972-38delinsAGGTCTAGCCT
XR_932842.2:n.2972-48_2972-38delinsAGGTCTAGCCT
XR_932846.3:n.2974-2_2982delinsAGGTCTAGCCT
XR_932847.3:n.2974-2_2982delinsAGGTCTAGCCT
NM_001286403.2:c.860-2_868delinsAGGTCTAGCCT
NR_104444.2:n.1136-1207_1136-1197delinsAGGTCTAGCCT
NM_000246.4:c.2658-48_2658-38delinsAGGTCTAGCCT MANE Select NP_000237.2:n.2658-48_2658-38delinsAGGTCTAGCCT
NM_001379330.1:c.2514-48_2514-38delinsAGGTCTAGCCT NP_001366259.1:n.2514-48_2514-38delinsAGGTCTAGCCT
NM_001379331.1:c.2511-48_2511-38delinsAGGTCTAGCCT NP_001366260.1:n.2511-48_2511-38delinsAGGTCTAGCCT
NM_001379332.1:c.2661-48_2661-38delinsAGGTCTAGCCT NP_001366261.1:n.2661-48_2661-38delinsAGGTCTAGCCT
NM_001379333.1:c.2658-48_2658-38delinsAGGTCTAGCCT NP_001366262.1:n.2658-48_2658-38delinsAGGTCTAGCCT
NM_001379334.1:c.2589-48_2589-38delinsAGGTCTAGCCT NP_001366263.1:n.2589-48_2589-38delinsAGGTCTAGCCT
Search 100 bp 5'
Search 100 bp 3'