Canonical Allele Identifier: CA397041110

Gene: CA5A

Linked Data

• MyVariant Identifiers: chr16:g.87936045C>A (hg19) ; chr16:g.87902439C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902439C>A , CM000678.2:g.87902439C>A	GRCh38
NC_000016.9:g.87936045C>A , CM000678.1:g.87936045C>A	GRCh37
NC_000016.8:g.86493546C>A	NCBI36
NG_033227.1:g.39068G>T
NG_033227.2:g.39091G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000648022.1:c.541G>T	ENSP00000497934.1:p.Gly181Cys
ENST00000648177.1:c.422G>T	ENSP00000497626.1:p.Arg141Met
ENST00000649158.1:c.541G>T	ENSP00000496993.1:p.Gly181Cys
ENST00000649794.3:c.541G>T MANE Select	ENSP00000498065.2:p.Gly181Cys
ENST00000309893.3:c.541G>T	ENSP00000309649.2:p.Gly181Cys
NM_001739.1:c.541G>T	NP_001730.1:p.Gly181Cys
XM_011523309.1:c.541G>T	XP_011521611.1:p.Gly181Cys
XM_011523310.1:c.541G>T	XP_011521612.1:p.Gly181Cys
XR_933417.1:n.660G>T
NM_001739.2:c.541G>T MANE Select	NP_001730.1:p.Gly181Cys
XM_011523309.2:c.541G>T	XP_011521611.1:p.Gly181Cys
XM_017023646.1:c.541G>T	XP_016879135.1:p.Gly181Cys
XM_024450434.1:c.163G>T	XP_024306202.1:p.Gly55Cys
XR_002957839.1:n.666G>T
NM_001367225.1:c.541G>T	NP_001354154.1:p.Gly181Cys
NR_159798.1:n.620G>T
NR_159799.1:n.501G>T