Canonical Allele Identifier: CA1619762431

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847209A= , CM000668.2:g.32847209A=	GRCh38
NC_000006.11:g.32814986A= , CM000668.1:g.32814986A=	GRCh37
NC_000006.10:g.32922964A=	NCBI36
NG_011759.1:g.11763T=
NG_028165.1:g.2727T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1056-5T= (TAP1)	ENSP00000513708.1:n.*1056-5T=
ENST00000698421.1:c.*798-5T= (TAP1)	ENSP00000513709.1:n.*798-5T=
ENST00000698422.1:c.1715-5T= (TAP1)	ENSP00000513710.1:n.1715-5T=
ENST00000698423.1:c.1904-5T= (TAP1)	ENSP00000513711.1:n.1904-5T=
ENST00000698424.1:c.1775-5T= (TAP1)	ENSP00000513712.1:n.1775-5T=
ENST00000354258.5:c.1904-5T= (TAP1) MANE Select	ENSP00000346206.5:n.1904-5T=
ENST00000643049.2:c.449-5T= (TAP1)	ENSP00000494148.2:n.449-5T=
ENST00000643923.1:n.1340-5T= (TAP1)
ENST00000645078.1:n.1499-5T= (TAP1)
ENST00000354258.4:c.2084-5T= (TAP1)	ENSP00000346206.4:n.2084-5T=
ENST00000395330.5:c.-10+2935A= (PSMB9)	ENSP00000378739.1:n.-10+2935A=
ENST00000414474.5:c.-10+2339A= (PSMB9)	ENSP00000394363.1:n.-10+2339A=
ENST00000486332.1:n.1829-5T= (TAP1)
ENST00000487296.1:n.779T= (TAP1)
NM_000593.5:c.2084-5T= (TAP1)	NP_000584.2:n.2084-5T=
NM_001292022.1:c.1301-5T= (TAP1)	NP_001278951.1:n.1301-5T=
NM_001292022.2:c.1301-5T= (TAP1)	NP_001278951.1:n.1301-5T=
NM_000593.6:c.1904-5T= (TAP1) MANE Select	NP_000584.3:n.1904-5T=