Canonical Allele Identifier: CA2711372058

Gene: TAP1 PSMB9

Linked Data

• dbSNP Id: rs2127386685

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847226_32847230del , CM000668.2:g.32847226_32847230del	GRCh38
NC_000006.11:g.32815003_32815007del , CM000668.1:g.32815003_32815007del	GRCh37
NC_000006.10:g.32922981_32922985del	NCBI36
NG_011759.1:g.11745_11749del
NG_028165.1:g.2709_2713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1056-23_*1056-19del (TAP1)	ENSP00000513708.1:n.*1056-23_*1056-19del
ENST00000698421.1:c.*798-23_*798-19del (TAP1)	ENSP00000513709.1:n.*798-23_*798-19del
ENST00000698422.1:c.1715-23_1715-19del (TAP1)	ENSP00000513710.1:n.1715-23_1715-19del
ENST00000698423.1:c.1904-23_1904-19del (TAP1)	ENSP00000513711.1:n.1904-23_1904-19del
ENST00000698424.1:c.1775-23_1775-19del (TAP1)	ENSP00000513712.1:n.1775-23_1775-19del
ENST00000354258.5:c.1904-23_1904-19del (TAP1) MANE Select	ENSP00000346206.5:n.1904-23_1904-19del
ENST00000643049.2:c.449-23_449-19del (TAP1)	ENSP00000494148.2:n.449-23_449-19del
ENST00000643923.1:n.1340-23_1340-19del (TAP1)
ENST00000645078.1:n.1499-23_1499-19del (TAP1)
ENST00000354258.4:c.2084-23_2084-19del (TAP1)	ENSP00000346206.4:n.2084-23_2084-19del
ENST00000395330.5:c.-10+2952_-10+2956del (PSMB9)	ENSP00000378739.1:n.-10+2952_-10+2956del
ENST00000414474.5:c.-10+2356_-10+2360del (PSMB9)	ENSP00000394363.1:n.-10+2356_-10+2360del
ENST00000486332.1:n.1829-23_1829-19del (TAP1)
ENST00000487296.1:n.761_765del (TAP1)
NM_000593.5:c.2084-23_2084-19del (TAP1)	NP_000584.2:n.2084-23_2084-19del
NM_001292022.1:c.1301-23_1301-19del (TAP1)	NP_001278951.1:n.1301-23_1301-19del
NM_001292022.2:c.1301-23_1301-19del (TAP1)	NP_001278951.1:n.1301-23_1301-19del
NM_000593.6:c.1904-23_1904-19del (TAP1) MANE Select	NP_000584.3:n.1904-23_1904-19del