Canonical Allele Identifier: CA2207318976
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10902139C= , CM000678.2:g.10902139C= GRCh38
NC_000016.9:g.10995996C= , CM000678.1:g.10995996C= GRCh37
NC_000016.8:g.10903497C= NCBI36
NG_009628.1:g.29942C= , LRG_49:g.29942C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695879.1:n.608C=
ENST00000324288.14:c.583C= MANE Select ENSP00000316328.8:p.Pro195=
ENST00000324288.12:c.583C= ENSP00000316328.8:p.Pro195=
ENST00000381835.9:c.482-519C= ENSP00000371257.5:n.482-519C=
ENST00000537380.1:n.583C=
ENST00000570546.5:n.704C=
ENST00000571186.5:c.*304C= ENSP00000459829.1:n.*304C=
ENST00000573309.5:n.600-519C=
ENST00000576601.1:c.511C= ENSP00000459608.1:p.Pro171=
ENST00000611587.4:c.485-519C= ENSP00000483487.1:n.485-519C=
ENST00000618207.4:c.583C= ENSP00000484761.1:p.Pro195=
ENST00000618327.4:c.586C= ENSP00000485010.1:p.Pro196=
NM_000246.3:c.583C= , LRG_49t1:c.583C= NP_000237.2:p.Pro195=
NM_001286402.1:c.586C= NP_001273331.1:p.Pro196=
NM_001286403.1:c.482-519C= NP_001273332.1:n.482-519C=
NR_104444.1:n.716C=
XM_006720880.2:c.880C= XP_006720943.2:p.Pro294=
XM_011522484.1:c.880C= XP_011520786.1:p.Pro294=
XM_011522485.1:c.880C= XP_011520787.1:p.Pro294=
XM_011522486.1:c.880C= XP_011520788.1:p.Pro294=
XM_011522487.1:c.680-519C= XP_011520789.1:n.680-519C=
XM_011522488.1:c.631C= XP_011520790.1:p.Pro211=
XM_011522489.1:c.677-519C= XP_011520791.1:n.677-519C=
XM_011522490.1:c.628C= XP_011520792.1:p.Pro210=
XM_011522491.1:c.880C= XP_011520793.1:p.Pro294=
XM_011522492.1:c.586C= XP_011520794.1:p.Pro196=
XM_011522493.1:c.583C= XP_011520795.1:p.Pro195=
XM_011522494.1:c.514C= XP_011520796.1:p.Pro172=
XM_011522495.1:c.485-519C= XP_011520797.1:n.485-519C=
XM_011522496.1:c.482-519C= XP_011520798.1:n.482-519C=
XR_932841.1:n.895C=
XR_932842.1:n.895C=
XR_932843.1:n.895C=
XR_932846.1:n.895C=
XR_932847.1:n.895C=
XR_932848.1:n.632-519C=
XM_006720880.3:c.880C= XP_006720943.2:p.Pro294=
XM_011522484.3:c.880C= XP_011520786.1:p.Pro294=
XM_011522485.2:c.880C= XP_011520787.1:p.Pro294=
XM_011522486.2:c.880C= XP_011520788.1:p.Pro294=
XM_011522487.2:c.680-519C= XP_011520789.1:n.680-519C=
XM_011522488.2:c.631C= XP_011520790.1:p.Pro211=
XM_011522489.2:c.677-519C= XP_011520791.1:n.677-519C=
XM_011522490.2:c.628C= XP_011520792.1:p.Pro210=
XM_011522491.2:c.880C= XP_011520793.1:p.Pro294=
XM_011522492.2:c.586C= XP_011520794.1:p.Pro196=
XM_011522493.2:c.583C= XP_011520795.1:p.Pro195=
XM_011522494.2:c.514C= XP_011520796.1:p.Pro172=
XM_011522495.2:c.485-519C= XP_011520797.1:n.485-519C=
XM_011522496.2:c.482-519C= XP_011520798.1:n.482-519C=
XM_024450280.1:c.826C= XP_024306048.1:p.Pro276=
XM_024450281.1:c.725-519C= XP_024306049.1:n.725-519C=
XR_001751904.1:n.899C=
XR_932841.3:n.897C=
XR_932842.2:n.897C=
XR_932846.3:n.899C=
XR_932847.3:n.899C=
NM_001286403.2:c.482-519C= NP_001273332.1:n.482-519C=
NR_104444.2:n.712C=
NM_000246.4:c.583C= MANE Select NP_000237.2:p.Pro195=
NM_001379330.1:c.485-519C= NP_001366259.1:n.485-519C=
NM_001379331.1:c.482-519C= NP_001366260.1:n.482-519C=
NM_001379332.1:c.586C= NP_001366261.1:p.Pro196=
NM_001379333.1:c.583C= NP_001366262.1:p.Pro195=
NM_001379334.1:c.514C= NP_001366263.1:p.Pro172=