Canonical Allele Identifier: CA1619762427

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847202C= , CM000668.2:g.32847202C=	GRCh38
NC_000006.11:g.32814979C= , CM000668.1:g.32814979C=	GRCh37
NC_000006.10:g.32922957C=	NCBI36
NG_011759.1:g.11770G=
NG_028165.1:g.2734G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1058G= (TAP1)	ENSP00000513708.1:n.*1058G=
ENST00000698421.1:c.*800G= (TAP1)	ENSP00000513709.1:n.*800G=
ENST00000698422.1:c.1717G= (TAP1)	ENSP00000513710.1:p.Val573=
ENST00000698423.1:c.1906G= (TAP1)	ENSP00000513711.1:p.Val636=
ENST00000698424.1:c.1777G= (TAP1)	ENSP00000513712.1:p.Val593=
ENST00000354258.5:c.1906G= (TAP1) MANE Select	ENSP00000346206.5:p.Val636=
ENST00000643049.2:c.451G= (TAP1)	ENSP00000494148.2:p.Val151=
ENST00000643923.1:n.1342G= (TAP1)
ENST00000645078.1:n.1501G= (TAP1)
ENST00000354258.4:c.2086G= (TAP1)	ENSP00000346206.4:p.Val696=
ENST00000395330.5:c.-10+2928C= (PSMB9)	ENSP00000378739.1:n.-10+2928C=
ENST00000414474.5:c.-10+2332C= (PSMB9)	ENSP00000394363.1:n.-10+2332C=
ENST00000486332.1:n.1831G= (TAP1)
ENST00000487296.1:n.786G= (TAP1)
NM_000593.5:c.2086G= (TAP1)	NP_000584.2:p.Val696=
NM_001292022.1:c.1303G= (TAP1)	NP_001278951.1:p.Val435=
NM_001292022.2:c.1303G= (TAP1)	NP_001278951.1:p.Val435=
NM_000593.6:c.1906G= (TAP1) MANE Select	NP_000584.3:p.Val636=