Canonical Allele Identifier: CA725499714

Gene: CA5A

Linked Data

• dbSNP Id: rs1264233349
• MyVariant Identifiers: chr16:g.87936433_87936434del (hg19) ; chr16:g.87902827_87902828del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902830_87902831del , CM000678.2:g.87902830_87902831del	GRCh38
NC_000016.9:g.87936436_87936437del , CM000678.1:g.87936436_87936437del	GRCh37
NC_000016.8:g.86493937_86493938del	NCBI36
NG_033227.1:g.38679_38680del
NG_033227.2:g.38702_38703del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.460-308_460-307del	ENSP00000497934.1:n.460-308_460-307del
ENST00000648177.1:c.341-308_341-307del	ENSP00000497626.1:n.341-308_341-307del
ENST00000649158.1:c.460-308_460-307del	ENSP00000496993.1:n.460-308_460-307del
ENST00000649794.3:c.460-308_460-307del MANE Select	ENSP00000498065.2:n.460-308_460-307del
ENST00000309893.3:c.460-308_460-307del	ENSP00000309649.2:n.460-308_460-307del
NM_001739.1:c.460-308_460-307del	NP_001730.1:n.460-308_460-307del
XM_011523309.1:c.460-308_460-307del	XP_011521611.1:n.460-308_460-307del
XM_011523310.1:c.460-308_460-307del	XP_011521612.1:n.460-308_460-307del
XR_933417.1:n.579-308_579-307del
NM_001739.2:c.460-308_460-307del MANE Select	NP_001730.1:n.460-308_460-307del
XM_011523309.2:c.460-308_460-307del	XP_011521611.1:n.460-308_460-307del
XM_017023646.1:c.460-308_460-307del	XP_016879135.1:n.460-308_460-307del
XM_024450434.1:c.82-308_82-307del	XP_024306202.1:n.82-308_82-307del
XR_002957839.1:n.585-308_585-307del
NM_001367225.1:c.460-308_460-307del	NP_001354154.1:n.460-308_460-307del
NR_159798.1:n.539-308_539-307del
NR_159799.1:n.420-308_420-307del