Canonical Allele Identifier: CA1619762298

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847077G= , CM000668.2:g.32847077G=	GRCh38
NC_000006.11:g.32814854G= , CM000668.1:g.32814854G=	GRCh37
NC_000006.10:g.32922832G=	NCBI36
NG_011759.1:g.11895C=
NG_028165.1:g.2859C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1183C= (TAP1)	ENSP00000513708.1:n.*1183C=
ENST00000698421.1:c.*925C= (TAP1)	ENSP00000513709.1:n.*925C=
ENST00000698422.1:c.1842C= (TAP1)	ENSP00000513710.1:p.Ser614=
ENST00000698423.1:c.2031C= (TAP1)	ENSP00000513711.1:p.Ser677=
ENST00000698424.1:c.1902C= (TAP1)	ENSP00000513712.1:p.Ser634=
ENST00000354258.5:c.2031C= (TAP1) MANE Select	ENSP00000346206.5:p.Ser677=
ENST00000643049.2:c.576C= (TAP1)	ENSP00000494148.2:p.Ser192=
ENST00000643923.1:n.1467C= (TAP1)
ENST00000645078.1:n.1626C= (TAP1)
ENST00000354258.4:c.2211C= (TAP1)	ENSP00000346206.4:p.Ser737=
ENST00000395330.5:c.-10+2803G= (PSMB9)	ENSP00000378739.1:n.-10+2803G=
ENST00000414474.5:c.-10+2207G= (PSMB9)	ENSP00000394363.1:n.-10+2207G=
ENST00000486332.1:n.1956C= (TAP1)
ENST00000487296.1:n.911C= (TAP1)
NM_000593.5:c.2211C= (TAP1)	NP_000584.2:p.Ser737=
NM_001292022.1:c.1428C= (TAP1)	NP_001278951.1:p.Ser476=
NM_001292022.2:c.1428C= (TAP1)	NP_001278951.1:p.Ser476=
NM_000593.6:c.2031C= (TAP1) MANE Select	NP_000584.3:p.Ser677=