Canonical Allele Identifier: CA2207312962

Gene: CIITA

Linked Data

• dbSNP Id: rs2035907642

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10877220G>A , CM000678.2:g.10877220G>A	GRCh38
NC_000016.9:g.10971077G>A , CM000678.1:g.10971077G>A	GRCh37
NC_000016.8:g.10878578G>A	NCBI36
NG_009628.1:g.5023G>A , LRG_49:g.5023G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324288.14:c.-111G>A MANE Select	ENSP00000316328.8:n.-111G>A
ENST00000636238.1:c.-21+10901G>A	ENSP00000490205.1:n.-21+10901G>A
ENST00000637439.1:c.283+10648G>A	ENSP00000489907.1:n.283+10648G>A
ENST00000324288.12:c.-111G>A	ENSP00000316328.8:n.-111G>A
ENST00000381835.9:c.-111G>A	ENSP00000371257.5:n.-111G>A
ENST00000570546.5:n.11G>A
ENST00000573309.5:n.5G>A
ENST00000611587.4:c.-111G>A	ENSP00000483487.1:n.-111G>A
ENST00000618207.4:c.-111G>A	ENSP00000484761.1:n.-111G>A
ENST00000618327.4:c.-111G>A	ENSP00000485010.1:n.-111G>A
NM_000246.3:c.-111G>A , LRG_49t1:c.-111G>A	NP_000237.2:n.-111G>A
NM_001286402.1:c.-111G>A	NP_001273331.1:n.-111G>A
NM_001286403.1:c.-111G>A	NP_001273332.1:n.-111G>A
NR_104444.1:n.23G>A
XM_006720880.2:c.346+10648G>A	XP_006720943.2:n.346+10648G>A
XM_011522484.1:c.346+10648G>A	XP_011520786.1:n.346+10648G>A
XM_011522485.1:c.346+10648G>A	XP_011520787.1:n.346+10648G>A
XM_011522486.1:c.346+10648G>A	XP_011520788.1:n.346+10648G>A
XM_011522487.1:c.247+10648G>A	XP_011520789.1:n.247+10648G>A
XM_011522489.1:c.247+10648G>A	XP_011520791.1:n.247+10648G>A
XM_011522491.1:c.346+10648G>A	XP_011520793.1:n.346+10648G>A
XM_011522492.1:c.-111G>A	XP_011520794.1:n.-111G>A
XM_011522493.1:c.-111G>A	XP_011520795.1:n.-111G>A
XM_011522494.1:c.-21+10901G>A	XP_011520796.1:n.-21+10901G>A
XM_011522495.1:c.-111G>A	XP_011520797.1:n.-111G>A
XM_011522496.1:c.-111G>A	XP_011520798.1:n.-111G>A
XR_932841.1:n.361+10648G>A
XR_932842.1:n.361+10648G>A
XR_932843.1:n.361+10648G>A
XR_932846.1:n.361+10648G>A
XR_932847.1:n.361+10648G>A
XR_932848.1:n.40G>A
XR_933067.1:n.1162+11095C>T
XR_933068.1:n.1162+11095C>T
XM_006720880.3:c.346+10648G>A	XP_006720943.2:n.346+10648G>A
XM_011522484.3:c.346+10648G>A	XP_011520786.1:n.346+10648G>A
XM_011522485.2:c.346+10648G>A	XP_011520787.1:n.346+10648G>A
XM_011522486.2:c.346+10648G>A	XP_011520788.1:n.346+10648G>A
XM_011522487.2:c.247+10648G>A	XP_011520789.1:n.247+10648G>A
XM_011522489.2:c.247+10648G>A	XP_011520791.1:n.247+10648G>A
XM_011522491.2:c.346+10648G>A	XP_011520793.1:n.346+10648G>A
XM_011522492.2:c.-111G>A	XP_011520794.1:n.-111G>A
XM_011522493.2:c.-111G>A	XP_011520795.1:n.-111G>A
XM_011522494.2:c.-21+10901G>A	XP_011520796.1:n.-21+10901G>A
XM_011522495.2:c.-111G>A	XP_011520797.1:n.-111G>A
XM_011522496.2:c.-111G>A	XP_011520798.1:n.-111G>A
XM_024450280.1:c.-111G>A	XP_024306048.1:n.-111G>A
XM_024450281.1:c.-111G>A	XP_024306049.1:n.-111G>A
XR_001751904.1:n.365+10648G>A
XR_002957860.1:n.1246+11095C>T
XR_002957861.1:n.1246+11095C>T
XR_002957863.1:n.1442+5799C>T
XR_932841.3:n.363+10648G>A
XR_932842.2:n.363+10648G>A
XR_932846.3:n.365+10648G>A
XR_932847.3:n.365+10648G>A
NM_001286403.2:c.-111G>A	NP_001273332.1:n.-111G>A
NR_104444.2:n.19G>A
NM_000246.4:c.-111G>A MANE Select	NP_000237.2:n.-111G>A
NM_001379330.1:c.-111G>A	NP_001366259.1:n.-111G>A
NM_001379331.1:c.-111G>A	NP_001366260.1:n.-111G>A
NM_001379332.1:c.-111G>A	NP_001366261.1:n.-111G>A
NM_001379333.1:c.-111G>A	NP_001366262.1:n.-111G>A