Canonical Allele Identifier: CA823989959

Gene: TAP1 PSMB9

Linked Data

• dbSNP Id: rs1313602851
• MyVariant Identifiers: chr6:g.32816375del (hg19) ; chr6:g.32848598del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32848599del , CM000668.2:g.32848599del	GRCh38
NC_000006.11:g.32816376del , CM000668.1:g.32816376del	GRCh37
NC_000006.10:g.32924354del	NCBI36
NG_011759.1:g.10374del
NG_028165.1:g.1338del

Transcript Alleles

HGVS	Amino-acid change
ENST00000698420.1:c.*718+54del (TAP1)	ENSP00000513708.1:n.*718+54del
ENST00000698421.1:c.*460+54del (TAP1)	ENSP00000513709.1:n.*460+54del
ENST00000698422.1:c.1377+392del (TAP1)	ENSP00000513710.1:n.1377+392del
ENST00000698423.1:c.1566+54del (TAP1)	ENSP00000513711.1:n.1566+54del
ENST00000698424.1:c.1437+54del (TAP1)	ENSP00000513712.1:n.1437+54del
ENST00000354258.5:c.1566+54del (TAP1) MANE Select	ENSP00000346206.5:n.1566+54del
ENST00000643049.2:c.142-536del (TAP1)	ENSP00000494148.2:n.142-536del
ENST00000643923.1:n.1002+54del (TAP1)
ENST00000645078.1:n.1161+54del (TAP1)
ENST00000354258.4:c.1746+54del (TAP1)	ENSP00000346206.4:n.1746+54del
ENST00000395330.5:c.-10+4325del (PSMB9)	ENSP00000378739.1:n.-10+4325del
ENST00000414474.5:c.-10+3729del (PSMB9)	ENSP00000394363.1:n.-10+3729del
ENST00000486332.1:n.1491+54del (TAP1)
NM_000593.5:c.1746+54del (TAP1)	NP_000584.2:n.1746+54del
NM_001292022.1:c.963+54del (TAP1)	NP_001278951.1:n.963+54del
NM_001292022.2:c.963+54del (TAP1)	NP_001278951.1:n.963+54del
NM_000593.6:c.1566+54del (TAP1) MANE Select	NP_000584.3:n.1566+54del