Canonical Allele Identifier: CA1619757991

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32850969G= , CM000668.2:g.32850969G=	GRCh38
NC_000006.11:g.32818746G= , CM000668.1:g.32818746G=	GRCh37
NC_000006.10:g.32926724G=	NCBI36
NG_011759.1:g.8003C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*177C= (TAP1)	ENSP00000513708.1:n.*177C=
ENST00000698421.1:c.845-452C= (TAP1)	ENSP00000513709.1:n.845-452C=
ENST00000698422.1:c.1025C= (TAP1)	ENSP00000513710.1:p.Pro342=
ENST00000698423.1:c.1025C= (TAP1)	ENSP00000513711.1:p.Pro342=
ENST00000698424.1:c.1025C= (TAP1)	ENSP00000513712.1:p.Pro342=
ENST00000354258.5:c.1025C= (TAP1) MANE Select	ENSP00000346206.5:p.Pro342=
ENST00000643049.2:c.141+2527C= (TAP1)	ENSP00000494148.2:n.141+2527C=
ENST00000643923.1:n.461C= (TAP1)
ENST00000645078.1:n.620C= (TAP1)
ENST00000354258.4:c.1205C= (TAP1)	ENSP00000346206.4:p.Pro402=
ENST00000395330.5:c.-9-5169G= (PSMB9)	ENSP00000378739.1:n.-9-5169G=
ENST00000414474.5:c.-9-5169G= (PSMB9)	ENSP00000394363.1:n.-9-5169G=
NM_000593.5:c.1205C= (TAP1)	NP_000584.2:p.Pro402=
NM_001292022.1:c.422C= (TAP1)	NP_001278951.1:p.Pro141=
NM_001292022.2:c.422C= (TAP1)	NP_001278951.1:p.Pro141=
NM_000593.6:c.1025C= (TAP1) MANE Select	NP_000584.3:p.Pro342=