Canonical Allele Identifier: CA397042002

Gene: CA5A

Linked Data

• MyVariant Identifiers: chr16:g.87936116A>T (hg19) ; chr16:g.87902510A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902510A>T , CM000678.2:g.87902510A>T	GRCh38
NC_000016.9:g.87936116A>T , CM000678.1:g.87936116A>T	GRCh37
NC_000016.8:g.86493617A>T	NCBI36
NG_033227.1:g.38997T>A
NG_033227.2:g.39020T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.470T>A	ENSP00000497934.1:p.Val157Asp
ENST00000648177.1:c.351T>A	ENSP00000497626.1:p.Ser117Arg
ENST00000649158.1:c.470T>A	ENSP00000496993.1:p.Val157Asp
ENST00000649794.3:c.470T>A MANE Select	ENSP00000498065.2:p.Val157Asp
ENST00000309893.3:c.470T>A	ENSP00000309649.2:p.Val157Asp
NM_001739.1:c.470T>A	NP_001730.1:p.Val157Asp
XM_011523309.1:c.470T>A	XP_011521611.1:p.Val157Asp
XM_011523310.1:c.470T>A	XP_011521612.1:p.Val157Asp
XR_933417.1:n.589T>A
NM_001739.2:c.470T>A MANE Select	NP_001730.1:p.Val157Asp
XM_011523309.2:c.470T>A	XP_011521611.1:p.Val157Asp
XM_017023646.1:c.470T>A	XP_016879135.1:p.Val157Asp
XM_024450434.1:c.92T>A	XP_024306202.1:p.Val31Asp
XR_002957839.1:n.595T>A
NM_001367225.1:c.470T>A	NP_001354154.1:p.Val157Asp
NR_159798.1:n.549T>A
NR_159799.1:n.430T>A