Canonical Allele Identifier: CA1619762296

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847073A= , CM000668.2:g.32847073A=	GRCh38
NC_000006.11:g.32814850A= , CM000668.1:g.32814850A=	GRCh37
NC_000006.10:g.32922828A=	NCBI36
NG_011759.1:g.11899T=
NG_028165.1:g.2863T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1187T= (TAP1)	ENSP00000513708.1:n.*1187T=
ENST00000698421.1:c.*929T= (TAP1)	ENSP00000513709.1:n.*929T=
ENST00000698422.1:c.1846T= (TAP1)	ENSP00000513710.1:p.Leu616=
ENST00000698423.1:c.2035T= (TAP1)	ENSP00000513711.1:p.Leu679=
ENST00000698424.1:c.1906T= (TAP1)	ENSP00000513712.1:p.Leu636=
ENST00000354258.5:c.2035T= (TAP1) MANE Select	ENSP00000346206.5:p.Leu679=
ENST00000643049.2:c.580T= (TAP1)	ENSP00000494148.2:p.Leu194=
ENST00000643923.1:n.1471T= (TAP1)
ENST00000645078.1:n.1630T= (TAP1)
ENST00000354258.4:c.2215T= (TAP1)	ENSP00000346206.4:p.Leu739=
ENST00000395330.5:c.-10+2799A= (PSMB9)	ENSP00000378739.1:n.-10+2799A=
ENST00000414474.5:c.-10+2203A= (PSMB9)	ENSP00000394363.1:n.-10+2203A=
ENST00000486332.1:n.1960T= (TAP1)
ENST00000487296.1:n.915T= (TAP1)
NM_000593.5:c.2215T= (TAP1)	NP_000584.2:p.Leu739=
NM_001292022.1:c.1432T= (TAP1)	NP_001278951.1:p.Leu478=
NM_001292022.2:c.1432T= (TAP1)	NP_001278951.1:p.Leu478=
NM_000593.6:c.2035T= (TAP1) MANE Select	NP_000584.3:p.Leu679=