Canonical Allele Identifier: CA980253658
Gene: CA5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902351_87902352insA , CM000678.2:g.87902351_87902352insA GRCh38
NC_000016.9:g.87935957_87935958insA , CM000678.1:g.87935957_87935958insA GRCh37
NC_000016.8:g.86493458_86493459insA NCBI36
NG_033227.1:g.39155_39156insT
NG_033227.2:g.39178_39179insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000648022.1:c.555+73_555+74insT ENSP00000497934.1:n.555+73_555+74insT
ENST00000648177.1:c.436+73_436+74insT ENSP00000497626.1:n.436+73_436+74insT
ENST00000649158.1:c.555+73_555+74insT ENSP00000496993.1:n.555+73_555+74insT
ENST00000649794.3:c.555+73_555+74insT MANE Select ENSP00000498065.2:n.555+73_555+74insT
ENST00000309893.3:c.555+73_555+74insT ENSP00000309649.2:n.555+73_555+74insT
NM_001739.1:c.555+73_555+74insT NP_001730.1:n.555+73_555+74insT
XM_011523309.1:c.555+73_555+74insT XP_011521611.1:n.555+73_555+74insT
XM_011523310.1:c.555+73_555+74insT XP_011521612.1:n.555+73_555+74insT
XR_933417.1:n.674+73_674+74insT
NM_001739.2:c.555+73_555+74insT MANE Select NP_001730.1:n.555+73_555+74insT
XM_011523309.2:c.555+73_555+74insT XP_011521611.1:n.555+73_555+74insT
XM_017023646.1:c.555+73_555+74insT XP_016879135.1:n.555+73_555+74insT
XM_024450434.1:c.177+73_177+74insT XP_024306202.1:n.177+73_177+74insT
XR_002957839.1:n.680+73_680+74insT
NM_001367225.1:c.555+73_555+74insT NP_001354154.1:n.555+73_555+74insT
NR_159798.1:n.634+73_634+74insT
NR_159799.1:n.515+73_515+74insT