Canonical Allele Identifier: CA278871

Gene: CIITA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10907555G>A , CM000678.2:g.10907555G>A	GRCh38
NC_000016.9:g.11001412G>A , CM000678.1:g.11001412G>A	GRCh37
NC_000016.8:g.10908913G>A	NCBI36
NG_009628.1:g.35358G>A , LRG_49:g.35358G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695879.1:n.1957G>A
ENST00000324288.14:c.2063G>A MANE Select	ENSP00000316328.8:p.Trp688Ter
ENST00000324288.12:c.2063G>A	ENSP00000316328.8:p.Trp688Ter
ENST00000381835.9:c.860-1428G>A	ENSP00000371257.5:n.860-1428G>A
ENST00000537380.1:n.1007-2633G>A
ENST00000570546.5:n.2184G>A
ENST00000573309.5:n.2034G>A
ENST00000611587.4:c.1919G>A	ENSP00000483487.1:p.Trp640Ter
ENST00000618207.4:c.1007-2633G>A	ENSP00000484761.1:n.1007-2633G>A
ENST00000618327.4:c.2066G>A	ENSP00000485010.1:p.Trp689Ter
NM_000246.3:c.2063G>A , LRG_49t1:c.2063G>A	NP_000237.2:p.Trp688Ter
NM_001286402.1:c.2066G>A	NP_001273331.1:p.Trp689Ter
NM_001286403.1:c.860-1428G>A	NP_001273332.1:n.860-1428G>A
NR_104444.1:n.1140-2633G>A
XM_006720880.2:c.2360G>A	XP_006720943.2:p.Trp787Ter
XM_011522484.1:c.2360G>A	XP_011520786.1:p.Trp787Ter
XM_011522485.1:c.2360G>A	XP_011520787.1:p.Trp787Ter
XM_011522486.1:c.2360G>A	XP_011520788.1:p.Trp787Ter
XM_011522487.1:c.2114G>A	XP_011520789.1:p.Trp705Ter
XM_011522488.1:c.2111G>A	XP_011520790.1:p.Trp704Ter
XM_011522489.1:c.2111G>A	XP_011520791.1:p.Trp704Ter
XM_011522490.1:c.2108G>A	XP_011520792.1:p.Trp703Ter
XM_011522491.1:c.2360G>A	XP_011520793.1:p.Trp787Ter
XM_011522492.1:c.2066G>A	XP_011520794.1:p.Trp689Ter
XM_011522493.1:c.2063G>A	XP_011520795.1:p.Trp688Ter
XM_011522494.1:c.1994G>A	XP_011520796.1:p.Trp665Ter
XM_011522495.1:c.1919G>A	XP_011520797.1:p.Trp640Ter
XM_011522496.1:c.1916G>A	XP_011520798.1:p.Trp639Ter
XR_932841.1:n.2375G>A
XR_932842.1:n.2375G>A
XR_932843.1:n.2375G>A
XR_932846.1:n.2375G>A
XR_932847.1:n.2375G>A
XR_932848.1:n.1010-1428G>A
XM_006720880.3:c.2360G>A	XP_006720943.2:p.Trp787Ter
XM_011522484.3:c.2360G>A	XP_011520786.1:p.Trp787Ter
XM_011522485.2:c.2360G>A	XP_011520787.1:p.Trp787Ter
XM_011522486.2:c.2360G>A	XP_011520788.1:p.Trp787Ter
XM_011522487.2:c.2114G>A	XP_011520789.1:p.Trp705Ter
XM_011522488.2:c.2111G>A	XP_011520790.1:p.Trp704Ter
XM_011522489.2:c.2111G>A	XP_011520791.1:p.Trp704Ter
XM_011522490.2:c.2108G>A	XP_011520792.1:p.Trp703Ter
XM_011522491.2:c.2360G>A	XP_011520793.1:p.Trp787Ter
XM_011522492.2:c.2066G>A	XP_011520794.1:p.Trp689Ter
XM_011522493.2:c.2063G>A	XP_011520795.1:p.Trp688Ter
XM_011522494.2:c.1994G>A	XP_011520796.1:p.Trp665Ter
XM_011522495.2:c.1919G>A	XP_011520797.1:p.Trp640Ter
XM_011522496.2:c.1916G>A	XP_011520798.1:p.Trp639Ter
XM_024450280.1:c.2306G>A	XP_024306048.1:p.Trp769Ter
XM_024450281.1:c.2159G>A	XP_024306049.1:p.Trp720Ter
XR_001751904.1:n.2379G>A
XR_932841.3:n.2377G>A
XR_932842.2:n.2377G>A
XR_932846.3:n.2379G>A
XR_932847.3:n.2379G>A
NM_001286403.2:c.860-1428G>A	NP_001273332.1:n.860-1428G>A
NR_104444.2:n.1136-2633G>A
NM_000246.4:c.2063G>A MANE Select	NP_000237.2:p.Trp688Ter
NM_001379330.1:c.1919G>A	NP_001366259.1:p.Trp640Ter
NM_001379331.1:c.1916G>A	NP_001366260.1:p.Trp639Ter
NM_001379332.1:c.2066G>A	NP_001366261.1:p.Trp689Ter
NM_001379333.1:c.2063G>A	NP_001366262.1:p.Trp688Ter
NM_001379334.1:c.1994G>A	NP_001366263.1:p.Trp665Ter