Canonical Allele Identifier: CA211255

Gene: TAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32828974T= , CM000668.2:g.32828974T=	GRCh38
NC_000006.11:g.32796751T= , CM000668.1:g.32796751T=	GRCh37
NC_000006.10:g.32904729T=	NCBI36
NG_009793.4:g.14797A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001290043.2:c.1993A= MANE Select	NP_001276972.1:p.Thr665=
ENST00000374897.4:c.1993A= MANE Select	ENSP00000364032.3:p.Thr665=
NM_001290043.1:c.1993A=	NP_001276972.1:p.Thr665=
NM_018833.2:c.1932+426A=	NP_061313.2:n.1932+426A=
NM_018833.3:c.1932+426A=	NP_061313.2:n.1932+426A=
ENST00000374897.2:c.1993A=	ENSP00000364032.2:p.Thr665=
ENST00000374899.8:c.1932+426A=	ENSP00000364034.4:n.1932+426A=
ENST00000452392.2:c.1932+426A=	ENSP00000391806.2:n.1932+426A=
ENST00000464100.1:n.819A=
ENST00000485701.2:n.5922A=
ENST00000620123.4:c.1993A=	ENSP00000481712.1:p.Thr665=
ENST00000652259.1:c.1932+426A=	ENSP00000498827.1:n.1932+426A=
ENST00000698440.1:c.1993A=	ENSP00000513722.1:p.Thr665=
ENST00000698441.1:c.1804A=	ENSP00000513723.1:p.Thr602=
ENST00000698448.1:c.1993A=	ENSP00000513733.1:p.Thr665=
ENST00000698449.1:c.2026A=	ENSP00000513734.1:p.Thr676=
ENST00000705716.1:c.1987A=	ENSP00000516164.1:p.Thr663=