Canonical Allele Identifier: CA2207318791
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10902044C= , CM000678.2:g.10902044C= GRCh38
NC_000016.9:g.10995901C= , CM000678.1:g.10995901C= GRCh37
NC_000016.8:g.10903402C= NCBI36
NG_009628.1:g.29847C= , LRG_49:g.29847C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695879.1:n.513C=
ENST00000324288.14:c.488C= MANE Select ENSP00000316328.8:p.Pro163=
ENST00000637439.1:c.722C= ENSP00000489907.1:p.Pro241=
ENST00000324288.12:c.488C= ENSP00000316328.8:p.Pro163=
ENST00000381835.9:c.481+486C= ENSP00000371257.5:n.481+486C=
ENST00000537380.1:n.488C=
ENST00000570546.5:n.609C=
ENST00000571186.5:c.*209C= ENSP00000459829.1:n.*209C=
ENST00000573309.5:n.599+486C=
ENST00000576601.1:c.416C= ENSP00000459608.1:p.Pro139=
ENST00000611587.4:c.484+486C= ENSP00000483487.1:n.484+486C=
ENST00000618207.4:c.488C= ENSP00000484761.1:p.Pro163=
ENST00000618327.4:c.491C= ENSP00000485010.1:p.Pro164=
NM_000246.3:c.488C= , LRG_49t1:c.488C= NP_000237.2:p.Pro163=
NM_001286402.1:c.491C= NP_001273331.1:p.Pro164=
NM_001286403.1:c.481+486C= NP_001273332.1:n.481+486C=
NR_104444.1:n.621C=
XM_006720880.2:c.785C= XP_006720943.2:p.Pro262=
XM_011522484.1:c.785C= XP_011520786.1:p.Pro262=
XM_011522485.1:c.785C= XP_011520787.1:p.Pro262=
XM_011522486.1:c.785C= XP_011520788.1:p.Pro262=
XM_011522487.1:c.679+486C= XP_011520789.1:n.679+486C=
XM_011522488.1:c.536C= XP_011520790.1:p.Pro179=
XM_011522489.1:c.676+486C= XP_011520791.1:n.676+486C=
XM_011522490.1:c.533C= XP_011520792.1:p.Pro178=
XM_011522491.1:c.785C= XP_011520793.1:p.Pro262=
XM_011522492.1:c.491C= XP_011520794.1:p.Pro164=
XM_011522493.1:c.488C= XP_011520795.1:p.Pro163=
XM_011522494.1:c.419C= XP_011520796.1:p.Pro140=
XM_011522495.1:c.484+486C= XP_011520797.1:n.484+486C=
XM_011522496.1:c.481+486C= XP_011520798.1:n.481+486C=
XR_932841.1:n.800C=
XR_932842.1:n.800C=
XR_932843.1:n.800C=
XR_932846.1:n.800C=
XR_932847.1:n.800C=
XR_932848.1:n.631+486C=
XM_006720880.3:c.785C= XP_006720943.2:p.Pro262=
XM_011522484.3:c.785C= XP_011520786.1:p.Pro262=
XM_011522485.2:c.785C= XP_011520787.1:p.Pro262=
XM_011522486.2:c.785C= XP_011520788.1:p.Pro262=
XM_011522487.2:c.679+486C= XP_011520789.1:n.679+486C=
XM_011522488.2:c.536C= XP_011520790.1:p.Pro179=
XM_011522489.2:c.676+486C= XP_011520791.1:n.676+486C=
XM_011522490.2:c.533C= XP_011520792.1:p.Pro178=
XM_011522491.2:c.785C= XP_011520793.1:p.Pro262=
XM_011522492.2:c.491C= XP_011520794.1:p.Pro164=
XM_011522493.2:c.488C= XP_011520795.1:p.Pro163=
XM_011522494.2:c.419C= XP_011520796.1:p.Pro140=
XM_011522495.2:c.484+486C= XP_011520797.1:n.484+486C=
XM_011522496.2:c.481+486C= XP_011520798.1:n.481+486C=
XM_024450280.1:c.731C= XP_024306048.1:p.Pro244=
XM_024450281.1:c.724+486C= XP_024306049.1:n.724+486C=
XR_001751904.1:n.804C=
XR_932841.3:n.802C=
XR_932842.2:n.802C=
XR_932846.3:n.804C=
XR_932847.3:n.804C=
NM_001286403.2:c.481+486C= NP_001273332.1:n.481+486C=
NR_104444.2:n.617C=
NM_000246.4:c.488C= MANE Select NP_000237.2:p.Pro163=
NM_001379330.1:c.484+486C= NP_001366259.1:n.484+486C=
NM_001379331.1:c.481+486C= NP_001366260.1:n.481+486C=
NM_001379332.1:c.491C= NP_001366261.1:p.Pro164=
NM_001379333.1:c.488C= NP_001366262.1:p.Pro163=
NM_001379334.1:c.419C= NP_001366263.1:p.Pro140=