Canonical Allele Identifier: CA1619762306

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847085C= , CM000668.2:g.32847085C=	GRCh38
NC_000006.11:g.32814862C= , CM000668.1:g.32814862C=	GRCh37
NC_000006.10:g.32922840C=	NCBI36
NG_011759.1:g.11887G=
NG_028165.1:g.2851G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1175G= (TAP1)	ENSP00000513708.1:n.*1175G=
ENST00000698421.1:c.*917G= (TAP1)	ENSP00000513709.1:n.*917G=
ENST00000698422.1:c.1834G= (TAP1)	ENSP00000513710.1:p.Ala612=
ENST00000698423.1:c.2023G= (TAP1)	ENSP00000513711.1:p.Ala675=
ENST00000698424.1:c.1894G= (TAP1)	ENSP00000513712.1:p.Ala632=
ENST00000354258.5:c.2023G= (TAP1) MANE Select	ENSP00000346206.5:p.Ala675=
ENST00000643049.2:c.568G= (TAP1)	ENSP00000494148.2:p.Ala190=
ENST00000643923.1:n.1459G= (TAP1)
ENST00000645078.1:n.1618G= (TAP1)
ENST00000354258.4:c.2203G= (TAP1)	ENSP00000346206.4:p.Ala735=
ENST00000395330.5:c.-10+2811C= (PSMB9)	ENSP00000378739.1:n.-10+2811C=
ENST00000414474.5:c.-10+2215C= (PSMB9)	ENSP00000394363.1:n.-10+2215C=
ENST00000486332.1:n.1948G= (TAP1)
ENST00000487296.1:n.903G= (TAP1)
NM_000593.5:c.2203G= (TAP1)	NP_000584.2:p.Ala735=
NM_001292022.1:c.1420G= (TAP1)	NP_001278951.1:p.Ala474=
NM_001292022.2:c.1420G= (TAP1)	NP_001278951.1:p.Ala474=
NM_000593.6:c.2023G= (TAP1) MANE Select	NP_000584.3:p.Ala675=