Canonical Allele Identifier: CA1619762322

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847117A= , CM000668.2:g.32847117A=	GRCh38
NC_000006.11:g.32814894A= , CM000668.1:g.32814894A=	GRCh37
NC_000006.10:g.32922872A=	NCBI36
NG_011759.1:g.11855T=
NG_028165.1:g.2819T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1143T= (TAP1)	ENSP00000513708.1:n.*1143T=
ENST00000698421.1:c.*885T= (TAP1)	ENSP00000513709.1:n.*885T=
ENST00000698422.1:c.1802T= (TAP1)	ENSP00000513710.1:p.Leu601=
ENST00000698423.1:c.1991T= (TAP1)	ENSP00000513711.1:p.Leu664=
ENST00000698424.1:c.1862T= (TAP1)	ENSP00000513712.1:p.Leu621=
ENST00000354258.5:c.1991T= (TAP1) MANE Select	ENSP00000346206.5:p.Leu664=
ENST00000643049.2:c.536T= (TAP1)	ENSP00000494148.2:p.Leu179=
ENST00000643923.1:n.1427T= (TAP1)
ENST00000645078.1:n.1586T= (TAP1)
ENST00000354258.4:c.2171T= (TAP1)	ENSP00000346206.4:p.Leu724=
ENST00000395330.5:c.-10+2843A= (PSMB9)	ENSP00000378739.1:n.-10+2843A=
ENST00000414474.5:c.-10+2247A= (PSMB9)	ENSP00000394363.1:n.-10+2247A=
ENST00000486332.1:n.1916T= (TAP1)
ENST00000487296.1:n.871T= (TAP1)
NM_000593.5:c.2171T= (TAP1)	NP_000584.2:p.Leu724=
NM_001292022.1:c.1388T= (TAP1)	NP_001278951.1:p.Leu463=
NM_001292022.2:c.1388T= (TAP1)	NP_001278951.1:p.Leu463=
NM_000593.6:c.1991T= (TAP1) MANE Select	NP_000584.3:p.Leu664=