Canonical Allele Identifier: CA1619762308

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847091G= , CM000668.2:g.32847091G=	GRCh38
NC_000006.11:g.32814868G= , CM000668.1:g.32814868G=	GRCh37
NC_000006.10:g.32922846G=	NCBI36
NG_011759.1:g.11881C=
NG_028165.1:g.2845C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1169C= (TAP1)	ENSP00000513708.1:n.*1169C=
ENST00000698421.1:c.*911C= (TAP1)	ENSP00000513709.1:n.*911C=
ENST00000698422.1:c.1828C= (TAP1)	ENSP00000513710.1:p.Leu610=
ENST00000698423.1:c.2017C= (TAP1)	ENSP00000513711.1:p.Leu673=
ENST00000698424.1:c.1888C= (TAP1)	ENSP00000513712.1:p.Leu630=
ENST00000354258.5:c.2017C= (TAP1) MANE Select	ENSP00000346206.5:p.Leu673=
ENST00000643049.2:c.562C= (TAP1)	ENSP00000494148.2:p.Leu188=
ENST00000643923.1:n.1453C= (TAP1)
ENST00000645078.1:n.1612C= (TAP1)
ENST00000354258.4:c.2197C= (TAP1)	ENSP00000346206.4:p.Leu733=
ENST00000395330.5:c.-10+2817G= (PSMB9)	ENSP00000378739.1:n.-10+2817G=
ENST00000414474.5:c.-10+2221G= (PSMB9)	ENSP00000394363.1:n.-10+2221G=
ENST00000486332.1:n.1942C= (TAP1)
ENST00000487296.1:n.897C= (TAP1)
NM_000593.5:c.2197C= (TAP1)	NP_000584.2:p.Leu733=
NM_001292022.1:c.1414C= (TAP1)	NP_001278951.1:p.Leu472=
NM_001292022.2:c.1414C= (TAP1)	NP_001278951.1:p.Leu472=
NM_000593.6:c.2017C= (TAP1) MANE Select	NP_000584.3:p.Leu673=