Canonical Allele Identifier: CA725499698

Gene: CA5A

Linked Data

• dbSNP Id: rs1160735937
• MyVariant Identifiers: chr16:g.87936417C>G (hg19) ; chr16:g.87902811C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902811C>G , CM000678.2:g.87902811C>G	GRCh38
NC_000016.9:g.87936417C>G , CM000678.1:g.87936417C>G	GRCh37
NC_000016.8:g.86493918C>G	NCBI36
NG_033227.1:g.38696G>C
NG_033227.2:g.38719G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.460-291G>C	ENSP00000497934.1:n.460-291G>C
ENST00000648177.1:c.341-291G>C	ENSP00000497626.1:n.341-291G>C
ENST00000649158.1:c.460-291G>C	ENSP00000496993.1:n.460-291G>C
ENST00000649794.3:c.460-291G>C MANE Select	ENSP00000498065.2:n.460-291G>C
ENST00000309893.3:c.460-291G>C	ENSP00000309649.2:n.460-291G>C
NM_001739.1:c.460-291G>C	NP_001730.1:n.460-291G>C
XM_011523309.1:c.460-291G>C	XP_011521611.1:n.460-291G>C
XM_011523310.1:c.460-291G>C	XP_011521612.1:n.460-291G>C
XR_933417.1:n.579-291G>C
NM_001739.2:c.460-291G>C MANE Select	NP_001730.1:n.460-291G>C
XM_011523309.2:c.460-291G>C	XP_011521611.1:n.460-291G>C
XM_017023646.1:c.460-291G>C	XP_016879135.1:n.460-291G>C
XM_024450434.1:c.82-291G>C	XP_024306202.1:n.82-291G>C
XR_002957839.1:n.585-291G>C
NM_001367225.1:c.460-291G>C	NP_001354154.1:n.460-291G>C
NR_159798.1:n.539-291G>C
NR_159799.1:n.420-291G>C