Canonical Allele Identifier: CA2207327737
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10909090C= , CM000678.2:g.10909090C= GRCh38
NC_000016.9:g.11002947C= , CM000678.1:g.11002947C= GRCh37
NC_000016.8:g.10910448C= NCBI36
NG_009628.1:g.36893C= , LRG_49:g.36893C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324288.14:c.2719C= MANE Select ENSP00000316328.8:p.Leu907=
ENST00000324288.12:c.2719C= ENSP00000316328.8:p.Leu907=
ENST00000381835.9:c.967C= ENSP00000371257.5:p.Leu323=
ENST00000537380.1:n.1007-1098C=
ENST00000570546.5:n.3719C=
ENST00000618207.4:c.1007-1098C= ENSP00000484761.1:n.1007-1098C=
ENST00000618327.4:c.2722C= ENSP00000485010.1:p.Leu908=
NM_000246.3:c.2719C= , LRG_49t1:c.2719C= NP_000237.2:p.Leu907=
NM_001286402.1:c.2722C= NP_001273331.1:p.Leu908=
NM_001286403.1:c.967C= NP_001273332.1:p.Leu323=
NR_104444.1:n.1140-1098C=
XM_006720880.2:c.3016C= XP_006720943.2:p.Leu1006=
XM_011522484.1:c.3016C= XP_011520786.1:p.Leu1006=
XM_011522485.1:c.3016C= XP_011520787.1:p.Leu1006=
XM_011522486.1:c.3016C= XP_011520788.1:p.Leu1006=
XM_011522487.1:c.2770C= XP_011520789.1:p.Leu924=
XM_011522488.1:c.2767C= XP_011520790.1:p.Leu923=
XM_011522489.1:c.2767C= XP_011520791.1:p.Leu923=
XM_011522490.1:c.2764C= XP_011520792.1:p.Leu922=
XM_011522491.1:c.3016C= XP_011520793.1:p.Leu1006=
XM_011522492.1:c.2722C= XP_011520794.1:p.Leu908=
XM_011522493.1:c.2719C= XP_011520795.1:p.Leu907=
XM_011522494.1:c.2650C= XP_011520796.1:p.Leu884=
XM_011522495.1:c.2575C= XP_011520797.1:p.Leu859=
XM_011522496.1:c.2572C= XP_011520798.1:p.Leu858=
XR_932841.1:n.3031C=
XR_932842.1:n.3031C=
XR_932843.1:n.3031C=
XR_932846.1:n.3077C=
XR_932847.1:n.3077C=
XR_932848.1:n.1117C=
XM_006720880.3:c.3016C= XP_006720943.2:p.Leu1006=
XM_011522484.3:c.3016C= XP_011520786.1:p.Leu1006=
XM_011522485.2:c.3016C= XP_011520787.1:p.Leu1006=
XM_011522486.2:c.3016C= XP_011520788.1:p.Leu1006=
XM_011522487.2:c.2770C= XP_011520789.1:p.Leu924=
XM_011522488.2:c.2767C= XP_011520790.1:p.Leu923=
XM_011522489.2:c.2767C= XP_011520791.1:p.Leu923=
XM_011522490.2:c.2764C= XP_011520792.1:p.Leu922=
XM_011522491.2:c.3016C= XP_011520793.1:p.Leu1006=
XM_011522492.2:c.2722C= XP_011520794.1:p.Leu908=
XM_011522493.2:c.2719C= XP_011520795.1:p.Leu907=
XM_011522494.2:c.2650C= XP_011520796.1:p.Leu884=
XM_011522495.2:c.2575C= XP_011520797.1:p.Leu859=
XM_011522496.2:c.2572C= XP_011520798.1:p.Leu858=
XM_024450280.1:c.2962C= XP_024306048.1:p.Leu988=
XM_024450281.1:c.2815C= XP_024306049.1:p.Leu939=
XR_001751904.1:n.3081C=
XR_932841.3:n.3033C=
XR_932842.2:n.3033C=
XR_932846.3:n.3081C=
XR_932847.3:n.3081C=
NM_001286403.2:c.967C= NP_001273332.1:p.Leu323=
NR_104444.2:n.1136-1098C=
NM_000246.4:c.2719C= MANE Select NP_000237.2:p.Leu907=
NM_001379330.1:c.2575C= NP_001366259.1:p.Leu859=
NM_001379331.1:c.2572C= NP_001366260.1:p.Leu858=
NM_001379332.1:c.2722C= NP_001366261.1:p.Leu908=
NM_001379333.1:c.2719C= NP_001366262.1:p.Leu907=
NM_001379334.1:c.2650C= NP_001366263.1:p.Leu884=