Canonical Allele Identifier: CA394728175

Gene: CIITA

Linked Data

• dbSNP Id: rs2038810794
• MyVariant Identifiers: chr16:g.10995916C>T (hg19) ; chr16:g.10902059C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10902059C>T , CM000678.2:g.10902059C>T	GRCh38
NC_000016.9:g.10995916C>T , CM000678.1:g.10995916C>T	GRCh37
NC_000016.8:g.10903417C>T	NCBI36
NG_009628.1:g.29862C>T , LRG_49:g.29862C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695879.1:n.528C>T
ENST00000324288.14:c.503C>T MANE Select	ENSP00000316328.8:p.Thr168Ile
ENST00000637439.1:c.737C>T	ENSP00000489907.1:p.Thr246Ile
ENST00000324288.12:c.503C>T	ENSP00000316328.8:p.Thr168Ile
ENST00000381835.9:c.481+501C>T	ENSP00000371257.5:n.481+501C>T
ENST00000537380.1:n.503C>T
ENST00000570546.5:n.624C>T
ENST00000571186.5:c.*224C>T	ENSP00000459829.1:n.*224C>T
ENST00000573309.5:n.599+501C>T
ENST00000576601.1:c.431C>T	ENSP00000459608.1:p.Thr144Ile
ENST00000611587.4:c.484+501C>T	ENSP00000483487.1:n.484+501C>T
ENST00000618207.4:c.503C>T	ENSP00000484761.1:p.Thr168Ile
ENST00000618327.4:c.506C>T	ENSP00000485010.1:p.Thr169Ile
NM_000246.3:c.503C>T , LRG_49t1:c.503C>T	NP_000237.2:p.Thr168Ile
NM_001286402.1:c.506C>T	NP_001273331.1:p.Thr169Ile
NM_001286403.1:c.481+501C>T	NP_001273332.1:n.481+501C>T
NR_104444.1:n.636C>T
XM_006720880.2:c.800C>T	XP_006720943.2:p.Thr267Ile
XM_011522484.1:c.800C>T	XP_011520786.1:p.Thr267Ile
XM_011522485.1:c.800C>T	XP_011520787.1:p.Thr267Ile
XM_011522486.1:c.800C>T	XP_011520788.1:p.Thr267Ile
XM_011522487.1:c.679+501C>T	XP_011520789.1:n.679+501C>T
XM_011522488.1:c.551C>T	XP_011520790.1:p.Thr184Ile
XM_011522489.1:c.676+501C>T	XP_011520791.1:n.676+501C>T
XM_011522490.1:c.548C>T	XP_011520792.1:p.Thr183Ile
XM_011522491.1:c.800C>T	XP_011520793.1:p.Thr267Ile
XM_011522492.1:c.506C>T	XP_011520794.1:p.Thr169Ile
XM_011522493.1:c.503C>T	XP_011520795.1:p.Thr168Ile
XM_011522494.1:c.434C>T	XP_011520796.1:p.Thr145Ile
XM_011522495.1:c.484+501C>T	XP_011520797.1:n.484+501C>T
XM_011522496.1:c.481+501C>T	XP_011520798.1:n.481+501C>T
XR_932841.1:n.815C>T
XR_932842.1:n.815C>T
XR_932843.1:n.815C>T
XR_932846.1:n.815C>T
XR_932847.1:n.815C>T
XR_932848.1:n.631+501C>T
XM_006720880.3:c.800C>T	XP_006720943.2:p.Thr267Ile
XM_011522484.3:c.800C>T	XP_011520786.1:p.Thr267Ile
XM_011522485.2:c.800C>T	XP_011520787.1:p.Thr267Ile
XM_011522486.2:c.800C>T	XP_011520788.1:p.Thr267Ile
XM_011522487.2:c.679+501C>T	XP_011520789.1:n.679+501C>T
XM_011522488.2:c.551C>T	XP_011520790.1:p.Thr184Ile
XM_011522489.2:c.676+501C>T	XP_011520791.1:n.676+501C>T
XM_011522490.2:c.548C>T	XP_011520792.1:p.Thr183Ile
XM_011522491.2:c.800C>T	XP_011520793.1:p.Thr267Ile
XM_011522492.2:c.506C>T	XP_011520794.1:p.Thr169Ile
XM_011522493.2:c.503C>T	XP_011520795.1:p.Thr168Ile
XM_011522494.2:c.434C>T	XP_011520796.1:p.Thr145Ile
XM_011522495.2:c.484+501C>T	XP_011520797.1:n.484+501C>T
XM_011522496.2:c.481+501C>T	XP_011520798.1:n.481+501C>T
XM_024450280.1:c.746C>T	XP_024306048.1:p.Thr249Ile
XM_024450281.1:c.724+501C>T	XP_024306049.1:n.724+501C>T
XR_001751904.1:n.819C>T
XR_932841.3:n.817C>T
XR_932842.2:n.817C>T
XR_932846.3:n.819C>T
XR_932847.3:n.819C>T
NM_001286403.2:c.481+501C>T	NP_001273332.1:n.481+501C>T
NR_104444.2:n.632C>T
NM_000246.4:c.503C>T MANE Select	NP_000237.2:p.Thr168Ile
NM_001379330.1:c.484+501C>T	NP_001366259.1:n.484+501C>T
NM_001379331.1:c.481+501C>T	NP_001366260.1:n.481+501C>T
NM_001379332.1:c.506C>T	NP_001366261.1:p.Thr169Ile
NM_001379333.1:c.503C>T	NP_001366262.1:p.Thr168Ile
NM_001379334.1:c.434C>T	NP_001366263.1:p.Thr145Ile