Canonical Allele Identifier: CA397042018

Gene: CA5A

Linked Data

• gnomAD v4: 16-87902516-T-C
• MyVariant Identifiers: chr16:g.87936122T>C (hg19) ; chr16:g.87902516T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902516T>C , CM000678.2:g.87902516T>C	GRCh38
NC_000016.9:g.87936122T>C , CM000678.1:g.87936122T>C	GRCh37
NC_000016.8:g.86493623T>C	NCBI36
NG_033227.1:g.38991A>G
NG_033227.2:g.39014A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.464A>G	ENSP00000497934.1:p.His155Arg
ENST00000648177.1:c.345A>G	ENSP00000497626.1:p.Ala115=
ENST00000649158.1:c.464A>G	ENSP00000496993.1:p.His155Arg
ENST00000649794.3:c.464A>G MANE Select	ENSP00000498065.2:p.His155Arg
ENST00000309893.3:c.464A>G	ENSP00000309649.2:p.His155Arg
NM_001739.1:c.464A>G	NP_001730.1:p.His155Arg
XM_011523309.1:c.464A>G	XP_011521611.1:p.His155Arg
XM_011523310.1:c.464A>G	XP_011521612.1:p.His155Arg
XR_933417.1:n.583A>G
NM_001739.2:c.464A>G MANE Select	NP_001730.1:p.His155Arg
XM_011523309.2:c.464A>G	XP_011521611.1:p.His155Arg
XM_017023646.1:c.464A>G	XP_016879135.1:p.His155Arg
XM_024450434.1:c.86A>G	XP_024306202.1:p.His29Arg
XR_002957839.1:n.589A>G
NM_001367225.1:c.464A>G	NP_001354154.1:p.His155Arg
NR_159798.1:n.543A>G
NR_159799.1:n.424A>G