Canonical Allele Identifier: CA1087615336

Linked Data

dbSNP Id: rs1770462549

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32847008_32847010del , CM000668.2:g.32847008_32847010del GRCh38
NC_000006.11:g.32814785_32814787del , CM000668.1:g.32814785_32814787del GRCh37
NC_000006.10:g.32922763_32922765del NCBI36
NG_011759.1:g.11965_11967del
NG_028165.1:g.2929_2931del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698420.1:c.*1192+61_*1192+63del (TAP1) ENSP00000513708.1:n.*1192+61_*1192+63del
ENST00000698421.1:c.*934+61_*934+63del (TAP1) ENSP00000513709.1:n.*934+61_*934+63del
ENST00000698422.1:c.1851+61_1851+63del (TAP1) ENSP00000513710.1:n.1851+61_1851+63del
ENST00000698423.1:c.2040+61_2040+63del (TAP1) ENSP00000513711.1:n.2040+61_2040+63del
ENST00000698424.1:c.1911+61_1911+63del (TAP1) ENSP00000513712.1:n.1911+61_1911+63del
ENST00000354258.5:c.2040+61_2040+63del (TAP1) MANE Select ENSP00000346206.5:n.2040+61_2040+63del
ENST00000643049.2:c.585+61_585+63del (TAP1) ENSP00000494148.2:n.585+61_585+63del
ENST00000643923.1:n.1476+61_1476+63del (TAP1)
ENST00000645078.1:n.1635+61_1635+63del (TAP1)
ENST00000354258.4:c.2220+61_2220+63del (TAP1) ENSP00000346206.4:n.2220+61_2220+63del
ENST00000395330.5:c.-10+2734_-10+2736del (PSMB9) ENSP00000378739.1:n.-10+2734_-10+2736del
ENST00000414474.5:c.-10+2138_-10+2140del (PSMB9) ENSP00000394363.1:n.-10+2138_-10+2140del
ENST00000486332.1:n.1965+61_1965+63del (TAP1)
ENST00000487296.1:n.920+61_920+63del (TAP1)
NM_000593.5:c.2220+61_2220+63del (TAP1) NP_000584.2:n.2220+61_2220+63del
NM_001292022.1:c.1437+61_1437+63del (TAP1) NP_001278951.1:n.1437+61_1437+63del
NM_001292022.2:c.1437+61_1437+63del (TAP1) NP_001278951.1:n.1437+61_1437+63del
NM_000593.6:c.2040+61_2040+63del (TAP1) MANE Select NP_000584.3:n.2040+61_2040+63del