Canonical Allele Identifier: CA7899733

Gene: CIITA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10901533G>A , CM000678.2:g.10901533G>A	GRCh38
NC_000016.9:g.10995390G>A , CM000678.1:g.10995390G>A	GRCh37
NC_000016.8:g.10902891G>A	NCBI36
NG_009628.1:g.29336G>A , LRG_49:g.29336G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695879.1:n.481G>A
ENST00000324288.14:c.456G>A MANE Select	ENSP00000316328.8:p.Pro152=
ENST00000636238.1:c.387G>A	ENSP00000490205.1:p.Pro129=
ENST00000637439.1:c.690G>A	ENSP00000489907.1:p.Pro230=
ENST00000324288.12:c.456G>A	ENSP00000316328.8:p.Pro152=
ENST00000381835.9:c.456G>A	ENSP00000371257.5:p.Pro152=
ENST00000537380.1:n.456G>A
ENST00000570546.5:n.577G>A
ENST00000571186.5:c.456G>A	ENSP00000459829.1:p.Pro152=
ENST00000573309.5:n.574G>A
ENST00000576601.1:c.384G>A	ENSP00000459608.1:p.Pro128=
ENST00000611587.4:c.459G>A	ENSP00000483487.1:p.Pro153=
ENST00000618207.4:c.456G>A	ENSP00000484761.1:p.Pro152=
ENST00000618327.4:c.459G>A	ENSP00000485010.1:p.Pro153=
NM_000246.3:c.456G>A , LRG_49t1:c.456G>A	NP_000237.2:p.Pro152=
NM_001286402.1:c.459G>A	NP_001273331.1:p.Pro153=
NM_001286403.1:c.456G>A	NP_001273332.1:p.Pro152=
NR_104444.1:n.589G>A
XM_006720880.2:c.753G>A	XP_006720943.2:p.Pro251=
XM_011522484.1:c.753G>A	XP_011520786.1:p.Pro251=
XM_011522485.1:c.753G>A	XP_011520787.1:p.Pro251=
XM_011522486.1:c.753G>A	XP_011520788.1:p.Pro251=
XM_011522487.1:c.654G>A	XP_011520789.1:p.Pro218=
XM_011522488.1:c.504G>A	XP_011520790.1:p.Pro168=
XM_011522489.1:c.651G>A	XP_011520791.1:p.Pro217=
XM_011522490.1:c.501G>A	XP_011520792.1:p.Pro167=
XM_011522491.1:c.753G>A	XP_011520793.1:p.Pro251=
XM_011522492.1:c.459G>A	XP_011520794.1:p.Pro153=
XM_011522493.1:c.456G>A	XP_011520795.1:p.Pro152=
XM_011522494.1:c.387G>A	XP_011520796.1:p.Pro129=
XM_011522495.1:c.459G>A	XP_011520797.1:p.Pro153=
XM_011522496.1:c.456G>A	XP_011520798.1:p.Pro152=
XR_932841.1:n.768G>A
XR_932842.1:n.768G>A
XR_932843.1:n.768G>A
XR_932846.1:n.768G>A
XR_932847.1:n.768G>A
XR_932848.1:n.606G>A
XM_006720880.3:c.753G>A	XP_006720943.2:p.Pro251=
XM_011522484.3:c.753G>A	XP_011520786.1:p.Pro251=
XM_011522485.2:c.753G>A	XP_011520787.1:p.Pro251=
XM_011522486.2:c.753G>A	XP_011520788.1:p.Pro251=
XM_011522487.2:c.654G>A	XP_011520789.1:p.Pro218=
XM_011522488.2:c.504G>A	XP_011520790.1:p.Pro168=
XM_011522489.2:c.651G>A	XP_011520791.1:p.Pro217=
XM_011522490.2:c.501G>A	XP_011520792.1:p.Pro167=
XM_011522491.2:c.753G>A	XP_011520793.1:p.Pro251=
XM_011522492.2:c.459G>A	XP_011520794.1:p.Pro153=
XM_011522493.2:c.456G>A	XP_011520795.1:p.Pro152=
XM_011522494.2:c.387G>A	XP_011520796.1:p.Pro129=
XM_011522495.2:c.459G>A	XP_011520797.1:p.Pro153=
XM_011522496.2:c.456G>A	XP_011520798.1:p.Pro152=
XM_024450280.1:c.699G>A	XP_024306048.1:p.Pro233=
XM_024450281.1:c.699G>A	XP_024306049.1:p.Pro233=
XR_001751904.1:n.772G>A
XR_932841.3:n.770G>A
XR_932842.2:n.770G>A
XR_932846.3:n.772G>A
XR_932847.3:n.772G>A
NM_001286403.2:c.456G>A	NP_001273332.1:p.Pro152=
NR_104444.2:n.585G>A
NM_000246.4:c.456G>A MANE Select	NP_000237.2:p.Pro152=
NM_001379330.1:c.459G>A	NP_001366259.1:p.Pro153=
NM_001379331.1:c.456G>A	NP_001366260.1:p.Pro152=
NM_001379332.1:c.459G>A	NP_001366261.1:p.Pro153=
NM_001379333.1:c.456G>A	NP_001366262.1:p.Pro152=
NM_001379334.1:c.387G>A	NP_001366263.1:p.Pro129=