Canonical Allele Identifier: CA1619762425

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847198T= , CM000668.2:g.32847198T=	GRCh38
NC_000006.11:g.32814975T= , CM000668.1:g.32814975T=	GRCh37
NC_000006.10:g.32922953T=	NCBI36
NG_011759.1:g.11774A=
NG_028165.1:g.2738A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1062A= (TAP1)	ENSP00000513708.1:n.*1062A=
ENST00000698421.1:c.*804A= (TAP1)	ENSP00000513709.1:n.*804A=
ENST00000698422.1:c.1721A= (TAP1)	ENSP00000513710.1:p.Asp574=
ENST00000698423.1:c.1910A= (TAP1)	ENSP00000513711.1:p.Asp637=
ENST00000698424.1:c.1781A= (TAP1)	ENSP00000513712.1:p.Asp594=
ENST00000354258.5:c.1910A= (TAP1) MANE Select	ENSP00000346206.5:p.Asp637=
ENST00000643049.2:c.455A= (TAP1)	ENSP00000494148.2:p.Asp152=
ENST00000643923.1:n.1346A= (TAP1)
ENST00000645078.1:n.1505A= (TAP1)
ENST00000354258.4:c.2090A= (TAP1)	ENSP00000346206.4:p.Asp697=
ENST00000395330.5:c.-10+2924T= (PSMB9)	ENSP00000378739.1:n.-10+2924T=
ENST00000414474.5:c.-10+2328T= (PSMB9)	ENSP00000394363.1:n.-10+2328T=
ENST00000486332.1:n.1835A= (TAP1)
ENST00000487296.1:n.790A= (TAP1)
NM_000593.5:c.2090A= (TAP1)	NP_000584.2:p.Asp697=
NM_001292022.1:c.1307A= (TAP1)	NP_001278951.1:p.Asp436=
NM_001292022.2:c.1307A= (TAP1)	NP_001278951.1:p.Asp436=
NM_000593.6:c.1910A= (TAP1) MANE Select	NP_000584.3:p.Asp637=