Canonical Allele Identifier: CA2678189215

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32847264_32847265del , CM000668.2:g.32847264_32847265del GRCh38
NC_000006.11:g.32815041_32815042del , CM000668.1:g.32815041_32815042del GRCh37
NC_000006.10:g.32923019_32923020del NCBI36
NG_011759.1:g.11707_11708del
NG_028165.1:g.2671_2672del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698420.1:c.*1056-61_*1056-60del (TAP1) ENSP00000513708.1:n.*1056-61_*1056-60del
ENST00000698421.1:c.*798-61_*798-60del (TAP1) ENSP00000513709.1:n.*798-61_*798-60del
ENST00000698422.1:c.1715-61_1715-60del (TAP1) ENSP00000513710.1:n.1715-61_1715-60del
ENST00000698423.1:c.1904-61_1904-60del (TAP1) ENSP00000513711.1:n.1904-61_1904-60del
ENST00000698424.1:c.1775-61_1775-60del (TAP1) ENSP00000513712.1:n.1775-61_1775-60del
ENST00000354258.5:c.1904-61_1904-60del (TAP1) MANE Select ENSP00000346206.5:n.1904-61_1904-60del
ENST00000643049.2:c.449-61_449-60del (TAP1) ENSP00000494148.2:n.449-61_449-60del
ENST00000643923.1:n.1340-61_1340-60del (TAP1)
ENST00000645078.1:n.1499-61_1499-60del (TAP1)
ENST00000354258.4:c.2084-61_2084-60del (TAP1) ENSP00000346206.4:n.2084-61_2084-60del
ENST00000395330.5:c.-10+2990_-10+2991del (PSMB9) ENSP00000378739.1:n.-10+2990_-10+2991del
ENST00000414474.5:c.-10+2394_-10+2395del (PSMB9) ENSP00000394363.1:n.-10+2394_-10+2395del
ENST00000486332.1:n.1829-61_1829-60del (TAP1)
ENST00000487296.1:n.723_724del (TAP1)
NM_000593.5:c.2084-61_2084-60del (TAP1) NP_000584.2:n.2084-61_2084-60del
NM_001292022.1:c.1301-61_1301-60del (TAP1) NP_001278951.1:n.1301-61_1301-60del
NM_001292022.2:c.1301-61_1301-60del (TAP1) NP_001278951.1:n.1301-61_1301-60del
NM_000593.6:c.1904-61_1904-60del (TAP1) MANE Select NP_000584.3:n.1904-61_1904-60del