Canonical Allele Identifier: CA2678189099

Gene: TAP1 PSMB9

Linked Data

• gnomAD v4: 6-32847206-TGCAGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847210_32847214del , CM000668.2:g.32847210_32847214del	GRCh38
NC_000006.11:g.32814987_32814991del , CM000668.1:g.32814987_32814991del	GRCh37
NC_000006.10:g.32922965_32922969del	NCBI36
NG_011759.1:g.11761_11765del
NG_028165.1:g.2725_2729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1056-7_*1056-3del (TAP1)	ENSP00000513708.1:n.*1056-7_*1056-3del
ENST00000698421.1:c.*798-7_*798-3del (TAP1)	ENSP00000513709.1:n.*798-7_*798-3del
ENST00000698422.1:c.1715-7_1715-3del (TAP1)	ENSP00000513710.1:n.1715-7_1715-3del
ENST00000698423.1:c.1904-7_1904-3del (TAP1)	ENSP00000513711.1:n.1904-7_1904-3del
ENST00000698424.1:c.1775-7_1775-3del (TAP1)	ENSP00000513712.1:n.1775-7_1775-3del
ENST00000354258.5:c.1904-7_1904-3del (TAP1) MANE Select	ENSP00000346206.5:n.1904-7_1904-3del
ENST00000643049.2:c.449-7_449-3del (TAP1)	ENSP00000494148.2:n.449-7_449-3del
ENST00000643923.1:n.1340-7_1340-3del (TAP1)
ENST00000645078.1:n.1499-7_1499-3del (TAP1)
ENST00000354258.4:c.2084-7_2084-3del (TAP1)	ENSP00000346206.4:n.2084-7_2084-3del
ENST00000395330.5:c.-10+2936_-10+2940del (PSMB9)	ENSP00000378739.1:n.-10+2936_-10+2940del
ENST00000414474.5:c.-10+2340_-10+2344del (PSMB9)	ENSP00000394363.1:n.-10+2340_-10+2344del
ENST00000486332.1:n.1829-7_1829-3del (TAP1)
ENST00000487296.1:n.777_781del (TAP1)
NM_000593.5:c.2084-7_2084-3del (TAP1)	NP_000584.2:n.2084-7_2084-3del
NM_001292022.1:c.1301-7_1301-3del (TAP1)	NP_001278951.1:n.1301-7_1301-3del
NM_001292022.2:c.1301-7_1301-3del (TAP1)	NP_001278951.1:n.1301-7_1301-3del
NM_000593.6:c.1904-7_1904-3del (TAP1) MANE Select	NP_000584.3:n.1904-7_1904-3del