Canonical Allele Identifier: CA1619762295

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847070G= , CM000668.2:g.32847070G=	GRCh38
NC_000006.11:g.32814847G= , CM000668.1:g.32814847G=	GRCh37
NC_000006.10:g.32922825G=	NCBI36
NG_011759.1:g.11902C=
NG_028165.1:g.2866C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1190C= (TAP1)	ENSP00000513708.1:n.*1190C=
ENST00000698421.1:c.*932C= (TAP1)	ENSP00000513709.1:n.*932C=
ENST00000698422.1:c.1849C= (TAP1)	ENSP00000513710.1:p.Gln617=
ENST00000698423.1:c.2038C= (TAP1)	ENSP00000513711.1:p.Gln680=
ENST00000698424.1:c.1909C= (TAP1)	ENSP00000513712.1:p.Gln637=
ENST00000354258.5:c.2038C= (TAP1) MANE Select	ENSP00000346206.5:p.Gln680=
ENST00000643049.2:c.583C= (TAP1)	ENSP00000494148.2:p.Gln195=
ENST00000643923.1:n.1474C= (TAP1)
ENST00000645078.1:n.1633C= (TAP1)
ENST00000354258.4:c.2218C= (TAP1)	ENSP00000346206.4:p.Gln740=
ENST00000395330.5:c.-10+2796G= (PSMB9)	ENSP00000378739.1:n.-10+2796G=
ENST00000414474.5:c.-10+2200G= (PSMB9)	ENSP00000394363.1:n.-10+2200G=
ENST00000486332.1:n.1963C= (TAP1)
ENST00000487296.1:n.918C= (TAP1)
NM_000593.5:c.2218C= (TAP1)	NP_000584.2:p.Gln740=
NM_001292022.1:c.1435C= (TAP1)	NP_001278951.1:p.Gln479=
NM_001292022.2:c.1435C= (TAP1)	NP_001278951.1:p.Gln479=
NM_000593.6:c.2038C= (TAP1) MANE Select	NP_000584.3:p.Gln680=