Canonical Allele Identifier: CA1619758091

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32850997T= , CM000668.2:g.32850997T=	GRCh38
NC_000006.11:g.32818774T= , CM000668.1:g.32818774T=	GRCh37
NC_000006.10:g.32926752T=	NCBI36
NG_011759.1:g.7975A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*149A= (TAP1)	ENSP00000513708.1:n.*149A=
ENST00000698421.1:c.845-480A= (TAP1)	ENSP00000513709.1:n.845-480A=
ENST00000698422.1:c.997A= (TAP1)	ENSP00000513710.1:p.Ile333=
ENST00000698423.1:c.997A= (TAP1)	ENSP00000513711.1:p.Ile333=
ENST00000698424.1:c.997A= (TAP1)	ENSP00000513712.1:p.Ile333=
ENST00000354258.5:c.997A= (TAP1) MANE Select	ENSP00000346206.5:p.Ile333=
ENST00000643049.2:c.141+2499A= (TAP1)	ENSP00000494148.2:n.141+2499A=
ENST00000643923.1:n.433A= (TAP1)
ENST00000645078.1:n.592A= (TAP1)
ENST00000354258.4:c.1177A= (TAP1)	ENSP00000346206.4:p.Ile393=
ENST00000395330.5:c.-9-5141T= (PSMB9)	ENSP00000378739.1:n.-9-5141T=
ENST00000414474.5:c.-9-5141T= (PSMB9)	ENSP00000394363.1:n.-9-5141T=
NM_000593.5:c.1177A= (TAP1)	NP_000584.2:p.Ile393=
NM_001292022.1:c.394A= (TAP1)	NP_001278951.1:p.Ile132=
NM_001292022.2:c.394A= (TAP1)	NP_001278951.1:p.Ile132=
NM_000593.6:c.997A= (TAP1) MANE Select	NP_000584.3:p.Ile333=