Canonical Allele Identifier: CA624156147

Gene: CA5A

Linked Data

• dbSNP Id: rs1384607895
• gnomAD v2: 16-87936458-C-A
• gnomAD v3: 16-87902852-C-A
• gnomAD v4: 16-87902852-C-A
• MyVariant Identifiers: chr16:g.87936458C>A (hg19) ; chr16:g.87902852C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902852C>A , CM000678.2:g.87902852C>A	GRCh38
NC_000016.9:g.87936458C>A , CM000678.1:g.87936458C>A	GRCh37
NC_000016.8:g.86493959C>A	NCBI36
NG_033227.1:g.38655G>T
NG_033227.2:g.38678G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.460-332G>T	ENSP00000497934.1:n.460-332G>T
ENST00000648177.1:c.341-332G>T	ENSP00000497626.1:n.341-332G>T
ENST00000649158.1:c.460-332G>T	ENSP00000496993.1:n.460-332G>T
ENST00000649794.3:c.460-332G>T MANE Select	ENSP00000498065.2:n.460-332G>T
ENST00000309893.3:c.460-332G>T	ENSP00000309649.2:n.460-332G>T
NM_001739.1:c.460-332G>T	NP_001730.1:n.460-332G>T
XM_011523309.1:c.460-332G>T	XP_011521611.1:n.460-332G>T
XM_011523310.1:c.460-332G>T	XP_011521612.1:n.460-332G>T
XR_933417.1:n.579-332G>T
NM_001739.2:c.460-332G>T MANE Select	NP_001730.1:n.460-332G>T
XM_011523309.2:c.460-332G>T	XP_011521611.1:n.460-332G>T
XM_017023646.1:c.460-332G>T	XP_016879135.1:n.460-332G>T
XM_024450434.1:c.82-332G>T	XP_024306202.1:n.82-332G>T
XR_002957839.1:n.585-332G>T
NM_001367225.1:c.460-332G>T	NP_001354154.1:n.460-332G>T
NR_159798.1:n.539-332G>T
NR_159799.1:n.420-332G>T