Canonical Allele Identifier: CA394724657

Gene: CIITA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10923271C>T , CM000678.2:g.10923271C>T	GRCh38
NC_000016.9:g.11017128C>T , CM000678.1:g.11017128C>T	GRCh37
NC_000016.8:g.10924629C>T	NCBI36
NG_009628.1:g.51074C>T , LRG_49:g.51074C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000246.4:c.3361C>T MANE Select	NP_000237.2:p.Gln1121Ter
ENST00000324288.14:c.3361C>T MANE Select	ENSP00000316328.8:p.Gln1121Ter
NM_000246.3:c.3361C>T , LRG_49t1:c.3361C>T	NP_000237.2:p.Gln1121Ter
NM_001286402.1:c.3364C>T	NP_001273331.1:p.Gln1122Ter
NM_001286403.1:c.1609C>T	NP_001273332.1:p.Gln537Ter
NM_001286403.2:c.1609C>T	NP_001273332.1:p.Gln537Ter
NM_001379330.1:c.3217C>T	NP_001366259.1:p.Gln1073Ter
NM_001379331.1:c.3214C>T	NP_001366260.1:p.Gln1072Ter
NM_001379332.1:c.3364C>T	NP_001366261.1:p.Gln1122Ter
NM_001379333.1:c.3361C>T	NP_001366262.1:p.Gln1121Ter
NM_001379334.1:c.3292C>T	NP_001366263.1:p.Gln1098Ter
NR_104444.1:n.1684C>T
NR_104444.2:n.1680C>T
ENST00000324288.12:c.3361C>T	ENSP00000316328.8:p.Gln1121Ter
ENST00000381835.9:c.1609C>T	ENSP00000371257.5:p.Gln537Ter
ENST00000570546.5:n.4361C>T
ENST00000575513.1:n.347C>T
ENST00000618207.4:c.*489C>T	ENSP00000484761.1:n.*489C>T
ENST00000618327.4:c.3364C>T	ENSP00000485010.1:p.Gln1122Ter
ENST00000644232.1:c.212C>T
ENST00000646979.1:c.212C>T
XM_006720880.2:c.3658C>T	XP_006720943.2:p.Gln1220Ter
XM_006720880.3:c.3658C>T	XP_006720943.2:p.Gln1220Ter
XM_011522484.1:c.3658C>T	XP_011520786.1:p.Gln1220Ter
XM_011522484.3:c.3658C>T	XP_011520786.1:p.Gln1220Ter
XM_011522485.1:c.3658C>T	XP_011520787.1:p.Gln1220Ter
XM_011522485.2:c.3658C>T	XP_011520787.1:p.Gln1220Ter
XM_011522487.1:c.3412C>T	XP_011520789.1:p.Gln1138Ter
XM_011522487.2:c.3412C>T	XP_011520789.1:p.Gln1138Ter
XM_011522488.1:c.3409C>T	XP_011520790.1:p.Gln1137Ter
XM_011522488.2:c.3409C>T	XP_011520790.1:p.Gln1137Ter
XM_011522489.1:c.3409C>T	XP_011520791.1:p.Gln1137Ter
XM_011522489.2:c.3409C>T	XP_011520791.1:p.Gln1137Ter
XM_011522490.1:c.3406C>T	XP_011520792.1:p.Gln1136Ter
XM_011522490.2:c.3406C>T	XP_011520792.1:p.Gln1136Ter
XM_011522492.1:c.3364C>T	XP_011520794.1:p.Gln1122Ter
XM_011522492.2:c.3364C>T	XP_011520794.1:p.Gln1122Ter
XM_011522493.1:c.3361C>T	XP_011520795.1:p.Gln1121Ter
XM_011522493.2:c.3361C>T	XP_011520795.1:p.Gln1121Ter
XM_011522494.1:c.3292C>T	XP_011520796.1:p.Gln1098Ter
XM_011522494.2:c.3292C>T	XP_011520796.1:p.Gln1098Ter
XM_011522495.1:c.3217C>T	XP_011520797.1:p.Gln1073Ter
XM_011522495.2:c.3217C>T	XP_011520797.1:p.Gln1073Ter
XM_011522496.1:c.3214C>T	XP_011520798.1:p.Gln1072Ter
XM_011522496.2:c.3214C>T	XP_011520798.1:p.Gln1072Ter
XM_024450280.1:c.3604C>T	XP_024306048.1:p.Gln1202Ter
XM_024450281.1:c.3457C>T	XP_024306049.1:p.Gln1153Ter
XR_001751904.1:n.3723C>T
XR_932841.1:n.3673C>T
XR_932841.3:n.3675C>T
XR_932842.1:n.3673C>T
XR_932842.2:n.3675C>T
XR_932843.1:n.3673C>T
XR_932846.1:n.3719C>T
XR_932846.3:n.3723C>T
XR_932848.1:n.1759C>T