Canonical Allele Identifier: CA2678189168

Gene: TAP1 PSMB9

Linked Data

• gnomAD v4: 6-32847247-TGTGCACGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847248_32847255del , CM000668.2:g.32847248_32847255del	GRCh38
NC_000006.11:g.32815025_32815032del , CM000668.1:g.32815025_32815032del	GRCh37
NC_000006.10:g.32923003_32923010del	NCBI36
NG_011759.1:g.11717_11724del
NG_028165.1:g.2681_2688del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1056-51_*1056-44del (TAP1)	ENSP00000513708.1:n.*1056-51_*1056-44del
ENST00000698421.1:c.*798-51_*798-44del (TAP1)	ENSP00000513709.1:n.*798-51_*798-44del
ENST00000698422.1:c.1715-51_1715-44del (TAP1)	ENSP00000513710.1:n.1715-51_1715-44del
ENST00000698423.1:c.1904-51_1904-44del (TAP1)	ENSP00000513711.1:n.1904-51_1904-44del
ENST00000698424.1:c.1775-51_1775-44del (TAP1)	ENSP00000513712.1:n.1775-51_1775-44del
ENST00000354258.5:c.1904-51_1904-44del (TAP1) MANE Select	ENSP00000346206.5:n.1904-51_1904-44del
ENST00000643049.2:c.449-51_449-44del (TAP1)	ENSP00000494148.2:n.449-51_449-44del
ENST00000643923.1:n.1340-51_1340-44del (TAP1)
ENST00000645078.1:n.1499-51_1499-44del (TAP1)
ENST00000354258.4:c.2084-51_2084-44del (TAP1)	ENSP00000346206.4:n.2084-51_2084-44del
ENST00000395330.5:c.-10+2974_-10+2981del (PSMB9)	ENSP00000378739.1:n.-10+2974_-10+2981del
ENST00000414474.5:c.-10+2378_-10+2385del (PSMB9)	ENSP00000394363.1:n.-10+2378_-10+2385del
ENST00000486332.1:n.1829-51_1829-44del (TAP1)
ENST00000487296.1:n.733_740del (TAP1)
NM_000593.5:c.2084-51_2084-44del (TAP1)	NP_000584.2:n.2084-51_2084-44del
NM_001292022.1:c.1301-51_1301-44del (TAP1)	NP_001278951.1:n.1301-51_1301-44del
NM_001292022.2:c.1301-51_1301-44del (TAP1)	NP_001278951.1:n.1301-51_1301-44del
NM_000593.6:c.1904-51_1904-44del (TAP1) MANE Select	NP_000584.3:n.1904-51_1904-44del