Canonical Allele Identifier: CA7899696
Gene: CIITA HGNC NCBI

Linked Data

ClinVar Variation Id: 317679
ClinVar RCV Id: RCV000285263
dbSNP Id: rs140106499

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10898950C>T , CM000678.2:g.10898950C>T GRCh38
NC_000016.9:g.10992807C>T , CM000678.1:g.10992807C>T GRCh37
NC_000016.8:g.10900308C>T NCBI36
NG_009628.1:g.26753C>T , LRG_49:g.26753C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695878.1:n.732C>T
ENST00000695879.1:n.409C>T
ENST00000324288.14:c.384C>T MANE Select ENSP00000316328.8:p.Ile128=
ENST00000636238.1:c.315C>T ENSP00000490205.1:p.Ile105=
ENST00000637439.1:c.618C>T ENSP00000489907.1:p.Ile206=
ENST00000324288.12:c.384C>T ENSP00000316328.8:p.Ile128=
ENST00000381835.9:c.384C>T ENSP00000371257.5:p.Ile128=
ENST00000537380.1:n.384C>T
ENST00000570546.5:n.505C>T
ENST00000571186.5:c.384C>T ENSP00000459829.1:p.Ile128=
ENST00000573309.5:n.502C>T
ENST00000576601.1:c.312C>T ENSP00000459608.1:p.Ile104=
ENST00000611587.4:c.387C>T ENSP00000483487.1:p.Ile129=
ENST00000618207.4:c.384C>T ENSP00000484761.1:p.Ile128=
ENST00000618327.4:c.387C>T ENSP00000485010.1:p.Ile129=
NM_000246.3:c.384C>T , LRG_49t1:c.384C>T NP_000237.2:p.Ile128=
NM_001286402.1:c.387C>T NP_001273331.1:p.Ile129=
NM_001286403.1:c.384C>T NP_001273332.1:p.Ile128=
NR_104444.1:n.517C>T
XM_006720880.2:c.681C>T XP_006720943.2:p.Ile227=
XM_011522484.1:c.681C>T XP_011520786.1:p.Ile227=
XM_011522485.1:c.681C>T XP_011520787.1:p.Ile227=
XM_011522486.1:c.681C>T XP_011520788.1:p.Ile227=
XM_011522487.1:c.582C>T XP_011520789.1:p.Ile194=
XM_011522488.1:c.432C>T XP_011520790.1:p.Ile144=
XM_011522489.1:c.579C>T XP_011520791.1:p.Ile193=
XM_011522490.1:c.429C>T XP_011520792.1:p.Ile143=
XM_011522491.1:c.681C>T XP_011520793.1:p.Ile227=
XM_011522492.1:c.387C>T XP_011520794.1:p.Ile129=
XM_011522493.1:c.384C>T XP_011520795.1:p.Ile128=
XM_011522494.1:c.315C>T XP_011520796.1:p.Ile105=
XM_011522495.1:c.387C>T XP_011520797.1:p.Ile129=
XM_011522496.1:c.384C>T XP_011520798.1:p.Ile128=
XR_932841.1:n.696C>T
XR_932842.1:n.696C>T
XR_932843.1:n.696C>T
XR_932846.1:n.696C>T
XR_932847.1:n.696C>T
XR_932848.1:n.534C>T
XM_006720880.3:c.681C>T XP_006720943.2:p.Ile227=
XM_011522484.3:c.681C>T XP_011520786.1:p.Ile227=
XM_011522485.2:c.681C>T XP_011520787.1:p.Ile227=
XM_011522486.2:c.681C>T XP_011520788.1:p.Ile227=
XM_011522487.2:c.582C>T XP_011520789.1:p.Ile194=
XM_011522488.2:c.432C>T XP_011520790.1:p.Ile144=
XM_011522489.2:c.579C>T XP_011520791.1:p.Ile193=
XM_011522490.2:c.429C>T XP_011520792.1:p.Ile143=
XM_011522491.2:c.681C>T XP_011520793.1:p.Ile227=
XM_011522492.2:c.387C>T XP_011520794.1:p.Ile129=
XM_011522493.2:c.384C>T XP_011520795.1:p.Ile128=
XM_011522494.2:c.315C>T XP_011520796.1:p.Ile105=
XM_011522495.2:c.387C>T XP_011520797.1:p.Ile129=
XM_011522496.2:c.384C>T XP_011520798.1:p.Ile128=
XM_024450280.1:c.627C>T XP_024306048.1:p.Ile209=
XM_024450281.1:c.627C>T XP_024306049.1:p.Ile209=
XR_001751904.1:n.700C>T
XR_002957858.1:n.385-45G>A
XR_002957859.1:n.385-45G>A
XR_932841.3:n.698C>T
XR_932842.2:n.698C>T
XR_932846.3:n.700C>T
XR_932847.3:n.700C>T
NM_001286403.2:c.384C>T NP_001273332.1:p.Ile128=
NR_104444.2:n.513C>T
NM_000246.4:c.384C>T MANE Select NP_000237.2:p.Ile128=
NM_001379330.1:c.387C>T NP_001366259.1:p.Ile129=
NM_001379331.1:c.384C>T NP_001366260.1:p.Ile128=
NM_001379332.1:c.387C>T NP_001366261.1:p.Ile129=
NM_001379333.1:c.384C>T NP_001366262.1:p.Ile128=
NM_001379334.1:c.315C>T NP_001366263.1:p.Ile105=