Canonical Allele Identifier: CA2678190774

Gene: TAP1 PSMB9

Linked Data

• gnomAD v4: 6-32848572-CAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32848573_32848575del , CM000668.2:g.32848573_32848575del	GRCh38
NC_000006.11:g.32816350_32816352del , CM000668.1:g.32816350_32816352del	GRCh37
NC_000006.10:g.32924328_32924330del	NCBI36
NG_011759.1:g.10397_10399del
NG_028165.1:g.1361_1363del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*718+77_*718+79del (TAP1)	ENSP00000513708.1:n.*718+77_*718+79del
ENST00000698421.1:c.*460+77_*460+79del (TAP1)	ENSP00000513709.1:n.*460+77_*460+79del
ENST00000698422.1:c.1377+415_1377+417del (TAP1)	ENSP00000513710.1:n.1377+415_1377+417del
ENST00000698423.1:c.1566+77_1566+79del (TAP1)	ENSP00000513711.1:n.1566+77_1566+79del
ENST00000698424.1:c.1437+77_1437+79del (TAP1)	ENSP00000513712.1:n.1437+77_1437+79del
ENST00000354258.5:c.1566+77_1566+79del (TAP1) MANE Select	ENSP00000346206.5:n.1566+77_1566+79del
ENST00000643049.2:c.142-513_142-511del (TAP1)	ENSP00000494148.2:n.142-513_142-511del
ENST00000643923.1:n.1002+77_1002+79del (TAP1)
ENST00000645078.1:n.1161+77_1161+79del (TAP1)
ENST00000354258.4:c.1746+77_1746+79del (TAP1)	ENSP00000346206.4:n.1746+77_1746+79del
ENST00000395330.5:c.-10+4299_-10+4301del (PSMB9)	ENSP00000378739.1:n.-10+4299_-10+4301del
ENST00000414474.5:c.-10+3703_-10+3705del (PSMB9)	ENSP00000394363.1:n.-10+3703_-10+3705del
ENST00000486332.1:n.1491+77_1491+79del (TAP1)
NM_000593.5:c.1746+77_1746+79del (TAP1)	NP_000584.2:n.1746+77_1746+79del
NM_001292022.1:c.963+77_963+79del (TAP1)	NP_001278951.1:n.963+77_963+79del
NM_001292022.2:c.963+77_963+79del (TAP1)	NP_001278951.1:n.963+77_963+79del
NM_000593.6:c.1566+77_1566+79del (TAP1) MANE Select	NP_000584.3:n.1566+77_1566+79del