Canonical Allele Identifier: CA1795135
Gene: COA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98608279C>T , CM000664.2:g.98608279C>T GRCh38
NC_000002.11:g.99224742C>T , CM000664.1:g.99224742C>T GRCh37
NC_000002.10:g.98591174C>T NCBI36
NG_031918.1:g.5240G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000328709.8:c.99+28G>A MANE Select ENSP00000330730.3:n.99+28G>A
ENST00000328709.7:c.99+28G>A ENSP00000330730.3:n.99+28G>A
ENST00000409997.1:c.99+28G>A ENSP00000386934.1:n.99+28G>A
ENST00000483527.5:n.229G>A
NM_001008215.2:c.99+28G>A NP_001008216.1:n.99+28G>A
NM_001008215.3:c.99+28G>A MANE Select NP_001008216.1:n.99+28G>A