Canonical Allele Identifier: CA2240759169
Gene: CA5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902439C= , CM000678.2:g.87902439C= GRCh38
NC_000016.9:g.87936045C= , CM000678.1:g.87936045C= GRCh37
NC_000016.8:g.86493546C= NCBI36
NG_033227.1:g.39068G=
NG_033227.2:g.39091G=

Transcript Alleles

HGVS Amino-acid change
ENST00000648022.1:c.541G= ENSP00000497934.1:p.Gly181=
ENST00000648177.1:c.422G= ENSP00000497626.1:p.Arg141=
ENST00000649158.1:c.541G= ENSP00000496993.1:p.Gly181=
ENST00000649794.3:c.541G= MANE Select ENSP00000498065.2:p.Gly181=
ENST00000309893.3:c.541G= ENSP00000309649.2:p.Gly181=
NM_001739.1:c.541G= NP_001730.1:p.Gly181=
XM_011523309.1:c.541G= XP_011521611.1:p.Gly181=
XM_011523310.1:c.541G= XP_011521612.1:p.Gly181=
XR_933417.1:n.660G=
NM_001739.2:c.541G= MANE Select NP_001730.1:p.Gly181=
XM_011523309.2:c.541G= XP_011521611.1:p.Gly181=
XM_017023646.1:c.541G= XP_016879135.1:p.Gly181=
XM_024450434.1:c.163G= XP_024306202.1:p.Gly55=
XR_002957839.1:n.666G=
NM_001367225.1:c.541G= NP_001354154.1:p.Gly181=
NR_159798.1:n.620G=
NR_159799.1:n.501G=