Canonical Allele Identifier: CA2207327753
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10909123G= , CM000678.2:g.10909123G= GRCh38
NC_000016.9:g.11002980G= , CM000678.1:g.11002980G= GRCh37
NC_000016.8:g.10910481G= NCBI36
NG_009628.1:g.36926G= , LRG_49:g.36926G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324288.14:c.2752G= MANE Select ENSP00000316328.8:p.Glu918=
ENST00000324288.12:c.2752G= ENSP00000316328.8:p.Glu918=
ENST00000381835.9:c.1000G= ENSP00000371257.5:p.Glu334=
ENST00000537380.1:n.1007-1065G=
ENST00000570546.5:n.3752G=
ENST00000618207.4:c.1007-1065G= ENSP00000484761.1:n.1007-1065G=
ENST00000618327.4:c.2755G= ENSP00000485010.1:p.Glu919=
NM_000246.3:c.2752G= , LRG_49t1:c.2752G= NP_000237.2:p.Glu918=
NM_001286402.1:c.2755G= NP_001273331.1:p.Glu919=
NM_001286403.1:c.1000G= NP_001273332.1:p.Glu334=
NR_104444.1:n.1140-1065G=
XM_006720880.2:c.3049G= XP_006720943.2:p.Glu1017=
XM_011522484.1:c.3049G= XP_011520786.1:p.Glu1017=
XM_011522485.1:c.3049G= XP_011520787.1:p.Glu1017=
XM_011522486.1:c.3049G= XP_011520788.1:p.Glu1017=
XM_011522487.1:c.2803G= XP_011520789.1:p.Glu935=
XM_011522488.1:c.2800G= XP_011520790.1:p.Glu934=
XM_011522489.1:c.2800G= XP_011520791.1:p.Glu934=
XM_011522490.1:c.2797G= XP_011520792.1:p.Glu933=
XM_011522491.1:c.3049G= XP_011520793.1:p.Glu1017=
XM_011522492.1:c.2755G= XP_011520794.1:p.Glu919=
XM_011522493.1:c.2752G= XP_011520795.1:p.Glu918=
XM_011522494.1:c.2683G= XP_011520796.1:p.Glu895=
XM_011522495.1:c.2608G= XP_011520797.1:p.Glu870=
XM_011522496.1:c.2605G= XP_011520798.1:p.Glu869=
XR_932841.1:n.3064G=
XR_932842.1:n.3064G=
XR_932843.1:n.3064G=
XR_932846.1:n.3110G=
XR_932847.1:n.3110G=
XR_932848.1:n.1150G=
XM_006720880.3:c.3049G= XP_006720943.2:p.Glu1017=
XM_011522484.3:c.3049G= XP_011520786.1:p.Glu1017=
XM_011522485.2:c.3049G= XP_011520787.1:p.Glu1017=
XM_011522486.2:c.3049G= XP_011520788.1:p.Glu1017=
XM_011522487.2:c.2803G= XP_011520789.1:p.Glu935=
XM_011522488.2:c.2800G= XP_011520790.1:p.Glu934=
XM_011522489.2:c.2800G= XP_011520791.1:p.Glu934=
XM_011522490.2:c.2797G= XP_011520792.1:p.Glu933=
XM_011522491.2:c.3049G= XP_011520793.1:p.Glu1017=
XM_011522492.2:c.2755G= XP_011520794.1:p.Glu919=
XM_011522493.2:c.2752G= XP_011520795.1:p.Glu918=
XM_011522494.2:c.2683G= XP_011520796.1:p.Glu895=
XM_011522495.2:c.2608G= XP_011520797.1:p.Glu870=
XM_011522496.2:c.2605G= XP_011520798.1:p.Glu869=
XM_024450280.1:c.2995G= XP_024306048.1:p.Glu999=
XM_024450281.1:c.2848G= XP_024306049.1:p.Glu950=
XR_001751904.1:n.3114G=
XR_932841.3:n.3066G=
XR_932842.2:n.3066G=
XR_932846.3:n.3114G=
XR_932847.3:n.3114G=
NM_001286403.2:c.1000G= NP_001273332.1:p.Glu334=
NR_104444.2:n.1136-1065G=
NM_000246.4:c.2752G= MANE Select NP_000237.2:p.Glu918=
NM_001379330.1:c.2608G= NP_001366259.1:p.Glu870=
NM_001379331.1:c.2605G= NP_001366260.1:p.Glu869=
NM_001379332.1:c.2755G= NP_001366261.1:p.Glu919=
NM_001379333.1:c.2752G= NP_001366262.1:p.Glu918=
NM_001379334.1:c.2683G= NP_001366263.1:p.Glu895=