Canonical Allele Identifier: CA1619757969

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32850951C= , CM000668.2:g.32850951C=	GRCh38
NC_000006.11:g.32818728C= , CM000668.1:g.32818728C=	GRCh37
NC_000006.10:g.32926706C=	NCBI36
NG_011759.1:g.8021G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*195G= (TAP1)	ENSP00000513708.1:n.*195G=
ENST00000698421.1:c.845-434G= (TAP1)	ENSP00000513709.1:n.845-434G=
ENST00000698422.1:c.1043G= (TAP1)	ENSP00000513710.1:p.Trp348=
ENST00000698423.1:c.1043G= (TAP1)	ENSP00000513711.1:p.Trp348=
ENST00000698424.1:c.1043G= (TAP1)	ENSP00000513712.1:p.Trp348=
ENST00000354258.5:c.1043G= (TAP1) MANE Select	ENSP00000346206.5:p.Trp348=
ENST00000643049.2:c.141+2545G= (TAP1)	ENSP00000494148.2:n.141+2545G=
ENST00000643923.1:n.479G= (TAP1)
ENST00000645078.1:n.638G= (TAP1)
ENST00000354258.4:c.1223G= (TAP1)	ENSP00000346206.4:p.Trp408=
ENST00000395330.5:c.-9-5187C= (PSMB9)	ENSP00000378739.1:n.-9-5187C=
ENST00000414474.5:c.-9-5187C= (PSMB9)	ENSP00000394363.1:n.-9-5187C=
NM_000593.5:c.1223G= (TAP1)	NP_000584.2:p.Trp408=
NM_001292022.1:c.440G= (TAP1)	NP_001278951.1:p.Trp147=
NM_001292022.2:c.440G= (TAP1)	NP_001278951.1:p.Trp147=
NM_000593.6:c.1043G= (TAP1) MANE Select	NP_000584.3:p.Trp348=