Canonical Allele Identifier: CA2207312966

Gene: CIITA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10877222G= , CM000678.2:g.10877222G=	GRCh38
NC_000016.9:g.10971079G= , CM000678.1:g.10971079G=	GRCh37
NC_000016.8:g.10878580G=	NCBI36
NG_009628.1:g.5025G= , LRG_49:g.5025G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324288.14:c.-109G= MANE Select	ENSP00000316328.8:n.-109G=
ENST00000636238.1:c.-21+10903G=	ENSP00000490205.1:n.-21+10903G=
ENST00000637439.1:c.283+10650G=	ENSP00000489907.1:n.283+10650G=
ENST00000324288.12:c.-109G=	ENSP00000316328.8:n.-109G=
ENST00000381835.9:c.-109G=	ENSP00000371257.5:n.-109G=
ENST00000570546.5:n.13G=
ENST00000573309.5:n.7G=
ENST00000611587.4:c.-109G=	ENSP00000483487.1:n.-109G=
ENST00000618207.4:c.-109G=	ENSP00000484761.1:n.-109G=
ENST00000618327.4:c.-109G=	ENSP00000485010.1:n.-109G=
NM_000246.3:c.-109G= , LRG_49t1:c.-109G=	NP_000237.2:n.-109G=
NM_001286402.1:c.-109G=	NP_001273331.1:n.-109G=
NM_001286403.1:c.-109G=	NP_001273332.1:n.-109G=
NR_104444.1:n.25G=
XM_006720880.2:c.346+10650G=	XP_006720943.2:n.346+10650G=
XM_011522484.1:c.346+10650G=	XP_011520786.1:n.346+10650G=
XM_011522485.1:c.346+10650G=	XP_011520787.1:n.346+10650G=
XM_011522486.1:c.346+10650G=	XP_011520788.1:n.346+10650G=
XM_011522487.1:c.247+10650G=	XP_011520789.1:n.247+10650G=
XM_011522489.1:c.247+10650G=	XP_011520791.1:n.247+10650G=
XM_011522491.1:c.346+10650G=	XP_011520793.1:n.346+10650G=
XM_011522492.1:c.-109G=	XP_011520794.1:n.-109G=
XM_011522493.1:c.-109G=	XP_011520795.1:n.-109G=
XM_011522494.1:c.-21+10903G=	XP_011520796.1:n.-21+10903G=
XM_011522495.1:c.-109G=	XP_011520797.1:n.-109G=
XM_011522496.1:c.-109G=	XP_011520798.1:n.-109G=
XR_932841.1:n.361+10650G=
XR_932842.1:n.361+10650G=
XR_932843.1:n.361+10650G=
XR_932846.1:n.361+10650G=
XR_932847.1:n.361+10650G=
XR_932848.1:n.42G=
XR_933067.1:n.1162+11093C=
XR_933068.1:n.1162+11093C=
XM_006720880.3:c.346+10650G=	XP_006720943.2:n.346+10650G=
XM_011522484.3:c.346+10650G=	XP_011520786.1:n.346+10650G=
XM_011522485.2:c.346+10650G=	XP_011520787.1:n.346+10650G=
XM_011522486.2:c.346+10650G=	XP_011520788.1:n.346+10650G=
XM_011522487.2:c.247+10650G=	XP_011520789.1:n.247+10650G=
XM_011522489.2:c.247+10650G=	XP_011520791.1:n.247+10650G=
XM_011522491.2:c.346+10650G=	XP_011520793.1:n.346+10650G=
XM_011522492.2:c.-109G=	XP_011520794.1:n.-109G=
XM_011522493.2:c.-109G=	XP_011520795.1:n.-109G=
XM_011522494.2:c.-21+10903G=	XP_011520796.1:n.-21+10903G=
XM_011522495.2:c.-109G=	XP_011520797.1:n.-109G=
XM_011522496.2:c.-109G=	XP_011520798.1:n.-109G=
XM_024450280.1:c.-109G=	XP_024306048.1:n.-109G=
XM_024450281.1:c.-109G=	XP_024306049.1:n.-109G=
XR_001751904.1:n.365+10650G=
XR_002957860.1:n.1246+11093C=
XR_002957861.1:n.1246+11093C=
XR_002957863.1:n.1442+5797C=
XR_932841.3:n.363+10650G=
XR_932842.2:n.363+10650G=
XR_932846.3:n.365+10650G=
XR_932847.3:n.365+10650G=
NM_001286403.2:c.-109G=	NP_001273332.1:n.-109G=
NR_104444.2:n.21G=
NM_000246.4:c.-109G= MANE Select	NP_000237.2:n.-109G=
NM_001379330.1:c.-109G=	NP_001366259.1:n.-109G=
NM_001379331.1:c.-109G=	NP_001366260.1:n.-109G=
NM_001379332.1:c.-109G=	NP_001366261.1:n.-109G=
NM_001379333.1:c.-109G=	NP_001366262.1:n.-109G=