Canonical Allele Identifier: CA496904623

Gene: CA5A

Linked Data

• COSMIC: COSM6080300
• MyVariant Identifiers: chr16:g.87936058A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902452A>T , CM000678.2:g.87902452A>T	GRCh38
NC_000016.9:g.87936058A>T , CM000678.1:g.87936058A>T	GRCh37
NC_000016.8:g.86493559A>T	NCBI36
NG_033227.1:g.39055T>A
NG_033227.2:g.39078T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.528T>A	ENSP00000497934.1:p.Gly176=
ENST00000648177.1:c.409T>A	ENSP00000497626.1:p.Phe137Ile
ENST00000649158.1:c.528T>A	ENSP00000496993.1:p.Gly176=
ENST00000649794.3:c.528T>A MANE Select	ENSP00000498065.2:p.Gly176=
ENST00000309893.3:c.528T>A	ENSP00000309649.2:p.Gly176=
NM_001739.1:c.528T>A	NP_001730.1:p.Gly176=
XM_011523309.1:c.528T>A	XP_011521611.1:p.Gly176=
XM_011523310.1:c.528T>A	XP_011521612.1:p.Gly176=
XR_933417.1:n.647T>A
NM_001739.2:c.528T>A MANE Select	NP_001730.1:p.Gly176=
XM_011523309.2:c.528T>A	XP_011521611.1:p.Gly176=
XM_017023646.1:c.528T>A	XP_016879135.1:p.Gly176=
XM_024450434.1:c.150T>A	XP_024306202.1:p.Gly50=
XR_002957839.1:n.653T>A
NM_001367225.1:c.528T>A	NP_001354154.1:p.Gly176=
NR_159798.1:n.607T>A
NR_159799.1:n.488T>A