Canonical Allele Identifier: CA1087616821

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32850920_32850921insTCTCG , CM000668.2:g.32850920_32850921insTCTCG GRCh38
NC_000006.11:g.32818697_32818698insTCTCG , CM000668.1:g.32818697_32818698insTCTCG GRCh37
NC_000006.10:g.32926675_32926676insTCTCG NCBI36
NG_011759.1:g.8051_8052insCGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000698420.1:c.*202+23_*202+24insCGAGA (TAP1) ENSP00000513708.1:n.*202+23_*202+24insCGAGA
ENST00000698421.1:c.845-404_845-403insCGAGA (TAP1) ENSP00000513709.1:n.845-404_845-403insCGAGA
ENST00000698422.1:c.1050+23_1050+24insCGAGA (TAP1) ENSP00000513710.1:n.1050+23_1050+24insCGAGA
ENST00000698423.1:c.1050+23_1050+24insCGAGA (TAP1) ENSP00000513711.1:n.1050+23_1050+24insCGAGA
ENST00000698424.1:c.1050+23_1050+24insCGAGA (TAP1) ENSP00000513712.1:n.1050+23_1050+24insCGAGA
ENST00000354258.5:c.1050+23_1050+24insCGAGA (TAP1) MANE Select ENSP00000346206.5:n.1050+23_1050+24insCGAGA
ENST00000643049.2:c.141+2575_141+2576insCGAGA (TAP1) ENSP00000494148.2:n.141+2575_141+2576insCGAGA
ENST00000643923.1:n.486+23_486+24insCGAGA (TAP1)
ENST00000645078.1:n.645+23_645+24insCGAGA (TAP1)
ENST00000354258.4:c.1230+23_1230+24insCGAGA (TAP1) ENSP00000346206.4:n.1230+23_1230+24insCGAGA
ENST00000395330.5:c.-9-5218_-9-5217insTCTCG (PSMB9) ENSP00000378739.1:n.-9-5218_-9-5217insTCTCG
ENST00000414474.5:c.-9-5218_-9-5217insTCTCG (PSMB9) ENSP00000394363.1:n.-9-5218_-9-5217insTCTCG
NM_000593.5:c.1230+23_1230+24insCGAGA (TAP1) NP_000584.2:n.1230+23_1230+24insCGAGA
NM_001292022.1:c.447+23_447+24insCGAGA (TAP1) NP_001278951.1:n.447+23_447+24insCGAGA
NM_001292022.2:c.447+23_447+24insCGAGA (TAP1) NP_001278951.1:n.447+23_447+24insCGAGA
NM_000593.6:c.1050+23_1050+24insCGAGA (TAP1) MANE Select NP_000584.3:n.1050+23_1050+24insCGAGA