Canonical Allele Identifier: CA496904609

Gene: CA5A

Linked Data

• gnomAD v4: 16-87902434-C-G
• MyVariant Identifiers: chr16:g.87936040C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902434C>G , CM000678.2:g.87902434C>G	GRCh38
NC_000016.9:g.87936040C>G , CM000678.1:g.87936040C>G	GRCh37
NC_000016.8:g.86493541C>G	NCBI36
NG_033227.1:g.39073G>C
NG_033227.2:g.39096G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.546G>C	ENSP00000497934.1:p.Val182=
ENST00000648177.1:c.427G>C	ENSP00000497626.1:p.Val143Leu
ENST00000649158.1:c.546G>C	ENSP00000496993.1:p.Val182=
ENST00000649794.3:c.546G>C MANE Select	ENSP00000498065.2:p.Val182=
ENST00000309893.3:c.546G>C	ENSP00000309649.2:p.Val182=
NM_001739.1:c.546G>C	NP_001730.1:p.Val182=
XM_011523309.1:c.546G>C	XP_011521611.1:p.Val182=
XM_011523310.1:c.546G>C	XP_011521612.1:p.Val182=
XR_933417.1:n.665G>C
NM_001739.2:c.546G>C MANE Select	NP_001730.1:p.Val182=
XM_011523309.2:c.546G>C	XP_011521611.1:p.Val182=
XM_017023646.1:c.546G>C	XP_016879135.1:p.Val182=
XM_024450434.1:c.168G>C	XP_024306202.1:p.Val56=
XR_002957839.1:n.671G>C
NM_001367225.1:c.546G>C	NP_001354154.1:p.Val182=
NR_159798.1:n.625G>C
NR_159799.1:n.506G>C