Canonical Allele Identifier: CA397041089

Gene: CA5A

Linked Data

• gnomAD v4: 16-87902433-A-C
• MyVariant Identifiers: chr16:g.87936039A>C (hg19) ; chr16:g.87902433A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902433A>C , CM000678.2:g.87902433A>C	GRCh38
NC_000016.9:g.87936039A>C , CM000678.1:g.87936039A>C	GRCh37
NC_000016.8:g.86493540A>C	NCBI36
NG_033227.1:g.39074T>G
NG_033227.2:g.39097T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.547T>G	ENSP00000497934.1:p.Phe183Val
ENST00000648177.1:c.428T>G	ENSP00000497626.1:p.Val143Gly
ENST00000649158.1:c.547T>G	ENSP00000496993.1:p.Phe183Val
ENST00000649794.3:c.547T>G MANE Select	ENSP00000498065.2:p.Phe183Val
ENST00000309893.3:c.547T>G	ENSP00000309649.2:p.Phe183Val
NM_001739.1:c.547T>G	NP_001730.1:p.Phe183Val
XM_011523309.1:c.547T>G	XP_011521611.1:p.Phe183Val
XM_011523310.1:c.547T>G	XP_011521612.1:p.Phe183Val
XR_933417.1:n.666T>G
NM_001739.2:c.547T>G MANE Select	NP_001730.1:p.Phe183Val
XM_011523309.2:c.547T>G	XP_011521611.1:p.Phe183Val
XM_017023646.1:c.547T>G	XP_016879135.1:p.Phe183Val
XM_024450434.1:c.169T>G	XP_024306202.1:p.Phe57Val
XR_002957839.1:n.672T>G
NM_001367225.1:c.547T>G	NP_001354154.1:p.Phe183Val
NR_159798.1:n.626T>G
NR_159799.1:n.507T>G