Canonical Allele Identifier: CA1087616852

Gene: TAP1 PSMB9

Linked Data

• gnomAD v3: 6-32850942-ACCTGGT-A
• gnomAD v4: 6-32850942-ACCTGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32850943_32850948del , CM000668.2:g.32850943_32850948del	GRCh38
NC_000006.11:g.32818720_32818725del , CM000668.1:g.32818720_32818725del	GRCh37
NC_000006.10:g.32926698_32926703del	NCBI36
NG_011759.1:g.8024_8029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*198_*202+1del (TAP1)
ENST00000698421.1:c.845-431_845-426del (TAP1)	ENSP00000513709.1:n.845-431_845-426del
ENST00000698422.1:c.1046_1050+1del (TAP1)
ENST00000698423.1:c.1046_1050+1del (TAP1)
ENST00000698424.1:c.1046_1050+1del (TAP1)
ENST00000354258.5:c.1046_1050+1del (TAP1)
ENST00000643049.2:c.141+2548_141+2553del (TAP1)	ENSP00000494148.2:n.141+2548_141+2553del
ENST00000643923.1:n.482_486+1del (TAP1)
ENST00000645078.1:n.641_645+1del (TAP1)
ENST00000354258.4:c.1226_1230+1del (TAP1)
ENST00000395330.5:c.-9-5195_-9-5190del (PSMB9)	ENSP00000378739.1:n.-9-5195_-9-5190del
ENST00000414474.5:c.-9-5195_-9-5190del (PSMB9)	ENSP00000394363.1:n.-9-5195_-9-5190del
NM_000593.5:c.1226_1230+1del (TAP1)
NM_001292022.1:c.443_447+1del (TAP1)
NM_001292022.2:c.443_447+1del (TAP1)
NM_000593.6:c.1046_1050+1del (TAP1)