Canonical Allele Identifier: CA2207327725

Gene: CIITA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10909070A= , CM000678.2:g.10909070A=	GRCh38
NC_000016.9:g.11002927A= , CM000678.1:g.11002927A=	GRCh37
NC_000016.8:g.10910428A=	NCBI36
NG_009628.1:g.36873A= , LRG_49:g.36873A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000246.4:c.2699A= MANE Select	NP_000237.2:p.Gln900=
ENST00000324288.14:c.2699A= MANE Select	ENSP00000316328.8:p.Gln900=
NM_000246.3:c.2699A= , LRG_49t1:c.2699A=	NP_000237.2:p.Gln900=
NM_001286402.1:c.2702A=	NP_001273331.1:p.Gln901=
NM_001286403.1:c.947A=	NP_001273332.1:p.Gln316=
NM_001286403.2:c.947A=	NP_001273332.1:p.Gln316=
NM_001379330.1:c.2555A=	NP_001366259.1:p.Gln852=
NM_001379331.1:c.2552A=	NP_001366260.1:p.Gln851=
NM_001379332.1:c.2702A=	NP_001366261.1:p.Gln901=
NM_001379333.1:c.2699A=	NP_001366262.1:p.Gln900=
NM_001379334.1:c.2630A=	NP_001366263.1:p.Gln877=
NR_104444.1:n.1140-1118A=
NR_104444.2:n.1136-1118A=
ENST00000324288.12:c.2699A=	ENSP00000316328.8:p.Gln900=
ENST00000381835.9:c.947A=	ENSP00000371257.5:p.Gln316=
ENST00000537380.1:n.1007-1118A=
ENST00000570546.5:n.3699A=
ENST00000618207.4:c.1007-1118A=	ENSP00000484761.1:n.1007-1118A=
ENST00000618327.4:c.2702A=	ENSP00000485010.1:p.Gln901=
XM_006720880.2:c.2996A=	XP_006720943.2:p.Gln999=
XM_006720880.3:c.2996A=	XP_006720943.2:p.Gln999=
XM_011522484.1:c.2996A=	XP_011520786.1:p.Gln999=
XM_011522484.3:c.2996A=	XP_011520786.1:p.Gln999=
XM_011522485.1:c.2996A=	XP_011520787.1:p.Gln999=
XM_011522485.2:c.2996A=	XP_011520787.1:p.Gln999=
XM_011522486.1:c.2996A=	XP_011520788.1:p.Gln999=
XM_011522486.2:c.2996A=	XP_011520788.1:p.Gln999=
XM_011522487.1:c.2750A=	XP_011520789.1:p.Gln917=
XM_011522487.2:c.2750A=	XP_011520789.1:p.Gln917=
XM_011522488.1:c.2747A=	XP_011520790.1:p.Gln916=
XM_011522488.2:c.2747A=	XP_011520790.1:p.Gln916=
XM_011522489.1:c.2747A=	XP_011520791.1:p.Gln916=
XM_011522489.2:c.2747A=	XP_011520791.1:p.Gln916=
XM_011522490.1:c.2744A=	XP_011520792.1:p.Gln915=
XM_011522490.2:c.2744A=	XP_011520792.1:p.Gln915=
XM_011522491.1:c.2996A=	XP_011520793.1:p.Gln999=
XM_011522491.2:c.2996A=	XP_011520793.1:p.Gln999=
XM_011522492.1:c.2702A=	XP_011520794.1:p.Gln901=
XM_011522492.2:c.2702A=	XP_011520794.1:p.Gln901=
XM_011522493.1:c.2699A=	XP_011520795.1:p.Gln900=
XM_011522493.2:c.2699A=	XP_011520795.1:p.Gln900=
XM_011522494.1:c.2630A=	XP_011520796.1:p.Gln877=
XM_011522494.2:c.2630A=	XP_011520796.1:p.Gln877=
XM_011522495.1:c.2555A=	XP_011520797.1:p.Gln852=
XM_011522495.2:c.2555A=	XP_011520797.1:p.Gln852=
XM_011522496.1:c.2552A=	XP_011520798.1:p.Gln851=
XM_011522496.2:c.2552A=	XP_011520798.1:p.Gln851=
XM_024450280.1:c.2942A=	XP_024306048.1:p.Gln981=
XM_024450281.1:c.2795A=	XP_024306049.1:p.Gln932=
XR_001751904.1:n.3061A=
XR_932841.1:n.3011A=
XR_932841.3:n.3013A=
XR_932842.1:n.3011A=
XR_932842.2:n.3013A=
XR_932843.1:n.3011A=
XR_932846.1:n.3057A=
XR_932846.3:n.3061A=
XR_932847.1:n.3057A=
XR_932847.3:n.3061A=
XR_932848.1:n.1097A=