Canonical Allele Identifier: CA397041164

Gene: CA5A

Linked Data

• MyVariant Identifiers: chr16:g.87936059C>A (hg19) ; chr16:g.87902453C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902453C>A , CM000678.2:g.87902453C>A	GRCh38
NC_000016.9:g.87936059C>A , CM000678.1:g.87936059C>A	GRCh37
NC_000016.8:g.86493560C>A	NCBI36
NG_033227.1:g.39054G>T
NG_033227.2:g.39077G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.527G>T	ENSP00000497934.1:p.Gly176Val
ENST00000648177.1:c.408G>T	ENSP00000497626.1:p.Trp136Cys
ENST00000649158.1:c.527G>T	ENSP00000496993.1:p.Gly176Val
ENST00000649794.3:c.527G>T MANE Select	ENSP00000498065.2:p.Gly176Val
ENST00000309893.3:c.527G>T	ENSP00000309649.2:p.Gly176Val
NM_001739.1:c.527G>T	NP_001730.1:p.Gly176Val
XM_011523309.1:c.527G>T	XP_011521611.1:p.Gly176Val
XM_011523310.1:c.527G>T	XP_011521612.1:p.Gly176Val
XR_933417.1:n.646G>T
NM_001739.2:c.527G>T MANE Select	NP_001730.1:p.Gly176Val
XM_011523309.2:c.527G>T	XP_011521611.1:p.Gly176Val
XM_017023646.1:c.527G>T	XP_016879135.1:p.Gly176Val
XM_024450434.1:c.149G>T	XP_024306202.1:p.Gly50Val
XR_002957839.1:n.652G>T
NM_001367225.1:c.527G>T	NP_001354154.1:p.Gly176Val
NR_159798.1:n.606G>T
NR_159799.1:n.487G>T