Canonical Allele Identifier: CA1619753325

Gene: TAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32829016G= , CM000668.2:g.32829016G=	GRCh38
NC_000006.11:g.32796793G= , CM000668.1:g.32796793G=	GRCh37
NC_000006.10:g.32904771G=	NCBI36
NG_009793.3:g.14755C=
NG_009793.4:g.14755C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485701.2:n.5880C=
ENST00000698440.1:c.1951C=	ENSP00000513722.1:p.Arg651=
ENST00000698441.1:c.1762C=	ENSP00000513723.1:p.Arg588=
ENST00000698448.1:c.1951C=	ENSP00000513733.1:p.Arg651=
ENST00000698449.1:c.1984C=	ENSP00000513734.1:p.Arg662=
ENST00000705716.1:c.1945C=	ENSP00000516164.1:p.Arg649=
ENST00000374897.4:c.1951C= MANE Select	ENSP00000364032.3:p.Arg651=
ENST00000652259.1:c.1932+384C=	ENSP00000498827.1:n.1932+384C=
ENST00000374897.2:c.1951C=	ENSP00000364032.2:p.Arg651=
ENST00000374899.8:c.1932+384C=	ENSP00000364034.4:n.1932+384C=
ENST00000452392.2:c.1932+384C=	ENSP00000391806.2:n.1932+384C=
ENST00000464100.1:n.777C=
ENST00000620123.4:c.1951C=	ENSP00000481712.1:p.Arg651=
NM_001290043.1:c.1951C=	NP_001276972.1:p.Arg651=
NM_018833.2:c.1932+384C=	NP_061313.2:n.1932+384C=
NM_001290043.2:c.1951C= MANE Select	NP_001276972.1:p.Arg651=
NM_018833.3:c.1932+384C=	NP_061313.2:n.1932+384C=