Canonical Allele Identifier: CA394734770

Gene: CIITA

Linked Data

• MyVariant Identifiers: chr16:g.11002920T>G (hg19) ; chr16:g.10909063T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10909063T>G , CM000678.2:g.10909063T>G	GRCh38
NC_000016.9:g.11002920T>G , CM000678.1:g.11002920T>G	GRCh37
NC_000016.8:g.10910421T>G	NCBI36
NG_009628.1:g.36866T>G , LRG_49:g.36866T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324288.14:c.2692T>G MANE Select	ENSP00000316328.8:p.Ser898Ala
ENST00000324288.12:c.2692T>G	ENSP00000316328.8:p.Ser898Ala
ENST00000381835.9:c.940T>G	ENSP00000371257.5:p.Ser314Ala
ENST00000537380.1:n.1007-1125T>G
ENST00000570546.5:n.3692T>G
ENST00000618207.4:c.1007-1125T>G	ENSP00000484761.1:n.1007-1125T>G
ENST00000618327.4:c.2695T>G	ENSP00000485010.1:p.Ser899Ala
NM_000246.3:c.2692T>G , LRG_49t1:c.2692T>G	NP_000237.2:p.Ser898Ala
NM_001286402.1:c.2695T>G	NP_001273331.1:p.Ser899Ala
NM_001286403.1:c.940T>G	NP_001273332.1:p.Ser314Ala
NR_104444.1:n.1140-1125T>G
XM_006720880.2:c.2989T>G	XP_006720943.2:p.Ser997Ala
XM_011522484.1:c.2989T>G	XP_011520786.1:p.Ser997Ala
XM_011522485.1:c.2989T>G	XP_011520787.1:p.Ser997Ala
XM_011522486.1:c.2989T>G	XP_011520788.1:p.Ser997Ala
XM_011522487.1:c.2743T>G	XP_011520789.1:p.Ser915Ala
XM_011522488.1:c.2740T>G	XP_011520790.1:p.Ser914Ala
XM_011522489.1:c.2740T>G	XP_011520791.1:p.Ser914Ala
XM_011522490.1:c.2737T>G	XP_011520792.1:p.Ser913Ala
XM_011522491.1:c.2989T>G	XP_011520793.1:p.Ser997Ala
XM_011522492.1:c.2695T>G	XP_011520794.1:p.Ser899Ala
XM_011522493.1:c.2692T>G	XP_011520795.1:p.Ser898Ala
XM_011522494.1:c.2623T>G	XP_011520796.1:p.Ser875Ala
XM_011522495.1:c.2548T>G	XP_011520797.1:p.Ser850Ala
XM_011522496.1:c.2545T>G	XP_011520798.1:p.Ser849Ala
XR_932841.1:n.3004T>G
XR_932842.1:n.3004T>G
XR_932843.1:n.3004T>G
XR_932846.1:n.3050T>G
XR_932847.1:n.3050T>G
XR_932848.1:n.1090T>G
XM_006720880.3:c.2989T>G	XP_006720943.2:p.Ser997Ala
XM_011522484.3:c.2989T>G	XP_011520786.1:p.Ser997Ala
XM_011522485.2:c.2989T>G	XP_011520787.1:p.Ser997Ala
XM_011522486.2:c.2989T>G	XP_011520788.1:p.Ser997Ala
XM_011522487.2:c.2743T>G	XP_011520789.1:p.Ser915Ala
XM_011522488.2:c.2740T>G	XP_011520790.1:p.Ser914Ala
XM_011522489.2:c.2740T>G	XP_011520791.1:p.Ser914Ala
XM_011522490.2:c.2737T>G	XP_011520792.1:p.Ser913Ala
XM_011522491.2:c.2989T>G	XP_011520793.1:p.Ser997Ala
XM_011522492.2:c.2695T>G	XP_011520794.1:p.Ser899Ala
XM_011522493.2:c.2692T>G	XP_011520795.1:p.Ser898Ala
XM_011522494.2:c.2623T>G	XP_011520796.1:p.Ser875Ala
XM_011522495.2:c.2548T>G	XP_011520797.1:p.Ser850Ala
XM_011522496.2:c.2545T>G	XP_011520798.1:p.Ser849Ala
XM_024450280.1:c.2935T>G	XP_024306048.1:p.Ser979Ala
XM_024450281.1:c.2788T>G	XP_024306049.1:p.Ser930Ala
XR_001751904.1:n.3054T>G
XR_932841.3:n.3006T>G
XR_932842.2:n.3006T>G
XR_932846.3:n.3054T>G
XR_932847.3:n.3054T>G
NM_001286403.2:c.940T>G	NP_001273332.1:p.Ser314Ala
NR_104444.2:n.1136-1125T>G
NM_000246.4:c.2692T>G MANE Select	NP_000237.2:p.Ser898Ala
NM_001379330.1:c.2548T>G	NP_001366259.1:p.Ser850Ala
NM_001379331.1:c.2545T>G	NP_001366260.1:p.Ser849Ala
NM_001379332.1:c.2695T>G	NP_001366261.1:p.Ser899Ala
NM_001379333.1:c.2692T>G	NP_001366262.1:p.Ser898Ala
NM_001379334.1:c.2623T>G	NP_001366263.1:p.Ser875Ala