Canonical Allele Identifier: CA2678189198

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32847260_32847262del , CM000668.2:g.32847260_32847262del GRCh38
NC_000006.11:g.32815037_32815039del , CM000668.1:g.32815037_32815039del GRCh37
NC_000006.10:g.32923015_32923017del NCBI36
NG_011759.1:g.11710_11712del
NG_028165.1:g.2674_2676del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698420.1:c.*1056-58_*1056-56del (TAP1) ENSP00000513708.1:n.*1056-58_*1056-56del
ENST00000698421.1:c.*798-58_*798-56del (TAP1) ENSP00000513709.1:n.*798-58_*798-56del
ENST00000698422.1:c.1715-58_1715-56del (TAP1) ENSP00000513710.1:n.1715-58_1715-56del
ENST00000698423.1:c.1904-58_1904-56del (TAP1) ENSP00000513711.1:n.1904-58_1904-56del
ENST00000698424.1:c.1775-58_1775-56del (TAP1) ENSP00000513712.1:n.1775-58_1775-56del
ENST00000354258.5:c.1904-58_1904-56del (TAP1) MANE Select ENSP00000346206.5:n.1904-58_1904-56del
ENST00000643049.2:c.449-58_449-56del (TAP1) ENSP00000494148.2:n.449-58_449-56del
ENST00000643923.1:n.1340-58_1340-56del (TAP1)
ENST00000645078.1:n.1499-58_1499-56del (TAP1)
ENST00000354258.4:c.2084-58_2084-56del (TAP1) ENSP00000346206.4:n.2084-58_2084-56del
ENST00000395330.5:c.-10+2986_-10+2988del (PSMB9) ENSP00000378739.1:n.-10+2986_-10+2988del
ENST00000414474.5:c.-10+2390_-10+2392del (PSMB9) ENSP00000394363.1:n.-10+2390_-10+2392del
ENST00000486332.1:n.1829-58_1829-56del (TAP1)
ENST00000487296.1:n.726_728del (TAP1)
NM_000593.5:c.2084-58_2084-56del (TAP1) NP_000584.2:n.2084-58_2084-56del
NM_001292022.1:c.1301-58_1301-56del (TAP1) NP_001278951.1:n.1301-58_1301-56del
NM_001292022.2:c.1301-58_1301-56del (TAP1) NP_001278951.1:n.1301-58_1301-56del
NM_000593.6:c.1904-58_1904-56del (TAP1) MANE Select NP_000584.3:n.1904-58_1904-56del