Canonical Allele Identifier: CA496898085

Gene: CA5A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87926869G>A , CM000678.2:g.87926869G>A	GRCh38
NC_000016.9:g.87960475G>A , CM000678.1:g.87960475G>A	GRCh37
NC_000016.8:g.86517976G>A	NCBI36
NG_033227.1:g.14638C>T
NG_033227.2:g.14661C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.219C>T	ENSP00000497934.1:p.Asp73=
ENST00000648177.1:c.219C>T	ENSP00000497626.1:p.Asp73=
ENST00000649158.1:c.219C>T	ENSP00000496993.1:p.Asp73=
ENST00000649794.3:c.219C>T MANE Select	ENSP00000498065.2:p.Asp73=
ENST00000309893.3:c.219C>T	ENSP00000309649.2:p.Asp73=
ENST00000568801.1:n.298C>T
NM_001739.1:c.219C>T	NP_001730.1:p.Asp73=
XM_005256134.3:c.219C>T	XP_005256191.1:p.Asp73=
XM_011523309.1:c.219C>T	XP_011521611.1:p.Asp73=
XM_011523310.1:c.219C>T	XP_011521612.1:p.Asp73=
XR_933417.1:n.338C>T
NM_001739.2:c.219C>T MANE Select	NP_001730.1:p.Asp73=
XM_005256134.4:c.219C>T	XP_005256191.1:p.Asp73=
XM_011523309.2:c.219C>T	XP_011521611.1:p.Asp73=
XM_017023646.1:c.219C>T	XP_016879135.1:p.Asp73=
XM_024450434.1:c.-41C>T	XP_024306202.1:n.-41C>T
XR_002957839.1:n.344C>T
NM_001367225.1:c.219C>T	NP_001354154.1:p.Asp73=
NR_159798.1:n.298C>T
NR_159799.1:n.298C>T