Canonical Allele Identifier: CA1619762399

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847176T= , CM000668.2:g.32847176T=	GRCh38
NC_000006.11:g.32814953T= , CM000668.1:g.32814953T=	GRCh37
NC_000006.10:g.32922931T=	NCBI36
NG_011759.1:g.11796A=
NG_028165.1:g.2760A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1084A= (TAP1)	ENSP00000513708.1:n.*1084A=
ENST00000698421.1:c.*826A= (TAP1)	ENSP00000513709.1:n.*826A=
ENST00000698422.1:c.1743A= (TAP1)	ENSP00000513710.1:p.Ser581=
ENST00000698423.1:c.1932A= (TAP1)	ENSP00000513711.1:p.Ser644=
ENST00000698424.1:c.1803A= (TAP1)	ENSP00000513712.1:p.Ser601=
ENST00000354258.5:c.1932A= (TAP1) MANE Select	ENSP00000346206.5:p.Ser644=
ENST00000643049.2:c.477A= (TAP1)	ENSP00000494148.2:p.Ser159=
ENST00000643923.1:n.1368A= (TAP1)
ENST00000645078.1:n.1527A= (TAP1)
ENST00000354258.4:c.2112A= (TAP1)	ENSP00000346206.4:p.Ser704=
ENST00000395330.5:c.-10+2902T= (PSMB9)	ENSP00000378739.1:n.-10+2902T=
ENST00000414474.5:c.-10+2306T= (PSMB9)	ENSP00000394363.1:n.-10+2306T=
ENST00000486332.1:n.1857A= (TAP1)
ENST00000487296.1:n.812A= (TAP1)
NM_000593.5:c.2112A= (TAP1)	NP_000584.2:p.Ser704=
NM_001292022.1:c.1329A= (TAP1)	NP_001278951.1:p.Ser443=
NM_001292022.2:c.1329A= (TAP1)	NP_001278951.1:p.Ser443=
NM_000593.6:c.1932A= (TAP1) MANE Select	NP_000584.3:p.Ser644=