Canonical Allele Identifier: CA1619754714

Gene: TAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32832461C= , CM000668.2:g.32832461C=	GRCh38
NC_000006.11:g.32800238C= , CM000668.1:g.32800238C=	GRCh37
NC_000006.10:g.32908216C=	NCBI36
NG_009793.3:g.11310G=
NG_009793.4:g.11310G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000485701.2:n.3547G=
ENST00000698440.1:c.1144G=	ENSP00000513722.1:p.Val382=
ENST00000698441.1:c.1144G=	ENSP00000513723.1:p.Val382=
ENST00000698448.1:c.1144G=	ENSP00000513733.1:p.Val382=
ENST00000698449.1:c.1144G=	ENSP00000513734.1:p.Val382=
ENST00000705716.1:c.1144G=	ENSP00000516164.1:p.Val382=
ENST00000374897.4:c.1144G= MANE Select	ENSP00000364032.3:p.Val382=
ENST00000652259.1:c.1144G=	ENSP00000498827.1:p.Val382=
ENST00000374897.2:c.1144G=	ENSP00000364032.2:p.Val382=
ENST00000374899.8:c.1144G=	ENSP00000364034.4:p.Val382=
ENST00000452392.2:c.1144G=	ENSP00000391806.2:p.Val382=
ENST00000485701.1:n.108G=
ENST00000620123.4:c.1144G=	ENSP00000481712.1:p.Val382=
NM_001290043.1:c.1144G=	NP_001276972.1:p.Val382=
NM_018833.2:c.1144G=	NP_061313.2:p.Val382=
NM_001290043.2:c.1144G= MANE Select	NP_001276972.1:p.Val382=
NM_018833.3:c.1144G=	NP_061313.2:p.Val382=