Canonical Allele Identifier: CA397041908

Gene: CA5A

Linked Data

• gnomAD v4: 16-87902487-G-C
• MyVariant Identifiers: chr16:g.87936093G>C (hg19) ; chr16:g.87902487G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902487G>C , CM000678.2:g.87902487G>C	GRCh38
NC_000016.9:g.87936093G>C , CM000678.1:g.87936093G>C	GRCh37
NC_000016.8:g.86493594G>C	NCBI36
NG_033227.1:g.39020C>G
NG_033227.2:g.39043C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.493C>G	ENSP00000497934.1:p.Gln165Glu
ENST00000648177.1:c.374C>G	ENSP00000497626.1:p.Pro125Arg
ENST00000649158.1:c.493C>G	ENSP00000496993.1:p.Gln165Glu
ENST00000649794.3:c.493C>G MANE Select	ENSP00000498065.2:p.Gln165Glu
ENST00000309893.3:c.493C>G	ENSP00000309649.2:p.Gln165Glu
NM_001739.1:c.493C>G	NP_001730.1:p.Gln165Glu
XM_011523309.1:c.493C>G	XP_011521611.1:p.Gln165Glu
XM_011523310.1:c.493C>G	XP_011521612.1:p.Gln165Glu
XR_933417.1:n.612C>G
NM_001739.2:c.493C>G MANE Select	NP_001730.1:p.Gln165Glu
XM_011523309.2:c.493C>G	XP_011521611.1:p.Gln165Glu
XM_017023646.1:c.493C>G	XP_016879135.1:p.Gln165Glu
XM_024450434.1:c.115C>G	XP_024306202.1:p.Gln39Glu
XR_002957839.1:n.618C>G
NM_001367225.1:c.493C>G	NP_001354154.1:p.Gln165Glu
NR_159798.1:n.572C>G
NR_159799.1:n.453C>G