Canonical Allele Identifier: CA2240759355
Gene: CA5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902773G= , CM000678.2:g.87902773G= GRCh38
NC_000016.9:g.87936379G= , CM000678.1:g.87936379G= GRCh37
NC_000016.8:g.86493880G= NCBI36
NG_033227.1:g.38734C=
NG_033227.2:g.38757C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648022.1:c.460-253C= ENSP00000497934.1:n.460-253C=
ENST00000648177.1:c.341-253C= ENSP00000497626.1:n.341-253C=
ENST00000649158.1:c.460-253C= ENSP00000496993.1:n.460-253C=
ENST00000649794.3:c.460-253C= MANE Select ENSP00000498065.2:n.460-253C=
ENST00000309893.3:c.460-253C= ENSP00000309649.2:n.460-253C=
NM_001739.1:c.460-253C= NP_001730.1:n.460-253C=
XM_011523309.1:c.460-253C= XP_011521611.1:n.460-253C=
XM_011523310.1:c.460-253C= XP_011521612.1:n.460-253C=
XR_933417.1:n.579-253C=
NM_001739.2:c.460-253C= MANE Select NP_001730.1:n.460-253C=
XM_011523309.2:c.460-253C= XP_011521611.1:n.460-253C=
XM_017023646.1:c.460-253C= XP_016879135.1:n.460-253C=
XM_024450434.1:c.82-253C= XP_024306202.1:n.82-253C=
XR_002957839.1:n.585-253C=
NM_001367225.1:c.460-253C= NP_001354154.1:n.460-253C=
NR_159798.1:n.539-253C=
NR_159799.1:n.420-253C=