Canonical Allele Identifier: CA397041911

Gene: CA5A

Linked Data

• MyVariant Identifiers: chr16:g.87936094G>C (hg19) ; chr16:g.87902488G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902488G>C , CM000678.2:g.87902488G>C	GRCh38
NC_000016.9:g.87936094G>C , CM000678.1:g.87936094G>C	GRCh37
NC_000016.8:g.86493595G>C	NCBI36
NG_033227.1:g.39019C>G
NG_033227.2:g.39042C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.492C>G	ENSP00000497934.1:p.Tyr164Ter
ENST00000648177.1:c.373C>G	ENSP00000497626.1:p.Pro125Ala
ENST00000649158.1:c.492C>G	ENSP00000496993.1:p.Tyr164Ter
ENST00000649794.3:c.492C>G MANE Select	ENSP00000498065.2:p.Tyr164Ter
ENST00000309893.3:c.492C>G	ENSP00000309649.2:p.Tyr164Ter
NM_001739.1:c.492C>G	NP_001730.1:p.Tyr164Ter
XM_011523309.1:c.492C>G	XP_011521611.1:p.Tyr164Ter
XM_011523310.1:c.492C>G	XP_011521612.1:p.Tyr164Ter
XR_933417.1:n.611C>G
NM_001739.2:c.492C>G MANE Select	NP_001730.1:p.Tyr164Ter
XM_011523309.2:c.492C>G	XP_011521611.1:p.Tyr164Ter
XM_017023646.1:c.492C>G	XP_016879135.1:p.Tyr164Ter
XM_024450434.1:c.114C>G	XP_024306202.1:p.Tyr38Ter
XR_002957839.1:n.617C>G
NM_001367225.1:c.492C>G	NP_001354154.1:p.Tyr164Ter
NR_159798.1:n.571C>G
NR_159799.1:n.452C>G