Canonical Allele Identifier: CA2634807027
Gene: CA5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902332_87902337del , CM000678.2:g.87902332_87902337del GRCh38
NC_000016.9:g.87935938_87935943del , CM000678.1:g.87935938_87935943del GRCh37
NC_000016.8:g.86493439_86493444del NCBI36
NG_033227.1:g.39170_39175del
NG_033227.2:g.39193_39198del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648022.1:c.555+88_555+93del ENSP00000497934.1:n.555+88_555+93del
ENST00000648177.1:c.436+88_436+93del ENSP00000497626.1:n.436+88_436+93del
ENST00000649158.1:c.555+88_555+93del ENSP00000496993.1:n.555+88_555+93del
ENST00000649794.3:c.555+88_555+93del MANE Select ENSP00000498065.2:n.555+88_555+93del
ENST00000309893.3:c.555+88_555+93del ENSP00000309649.2:n.555+88_555+93del
NM_001739.1:c.555+88_555+93del NP_001730.1:n.555+88_555+93del
XM_011523309.1:c.555+88_555+93del XP_011521611.1:n.555+88_555+93del
XM_011523310.1:c.555+88_555+93del XP_011521612.1:n.555+88_555+93del
XR_933417.1:n.674+88_674+93del
NM_001739.2:c.555+88_555+93del MANE Select NP_001730.1:n.555+88_555+93del
XM_011523309.2:c.555+88_555+93del XP_011521611.1:n.555+88_555+93del
XM_017023646.1:c.555+88_555+93del XP_016879135.1:n.555+88_555+93del
XM_024450434.1:c.177+88_177+93del XP_024306202.1:n.177+88_177+93del
XR_002957839.1:n.680+88_680+93del
NM_001367225.1:c.555+88_555+93del NP_001354154.1:n.555+88_555+93del
NR_159798.1:n.634+88_634+93del
NR_159799.1:n.515+88_515+93del