Canonical Allele Identifier: CA725499722

Gene: CA5A

Linked Data

• dbSNP Id: rs1286675132
• MyVariant Identifiers: chr16:g.87936436_87936440del (hg19) ; chr16:g.87902830_87902834del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902830_87902834del , CM000678.2:g.87902830_87902834del	GRCh38
NC_000016.9:g.87936436_87936440del , CM000678.1:g.87936436_87936440del	GRCh37
NC_000016.8:g.86493937_86493941del	NCBI36
NG_033227.1:g.38673_38677del
NG_033227.2:g.38696_38700del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.460-314_460-310del	ENSP00000497934.1:n.460-314_460-310del
ENST00000648177.1:c.341-314_341-310del	ENSP00000497626.1:n.341-314_341-310del
ENST00000649158.1:c.460-314_460-310del	ENSP00000496993.1:n.460-314_460-310del
ENST00000649794.3:c.460-314_460-310del MANE Select	ENSP00000498065.2:n.460-314_460-310del
ENST00000309893.3:c.460-314_460-310del	ENSP00000309649.2:n.460-314_460-310del
NM_001739.1:c.460-314_460-310del	NP_001730.1:n.460-314_460-310del
XM_011523309.1:c.460-314_460-310del	XP_011521611.1:n.460-314_460-310del
XM_011523310.1:c.460-314_460-310del	XP_011521612.1:n.460-314_460-310del
XR_933417.1:n.579-314_579-310del
NM_001739.2:c.460-314_460-310del MANE Select	NP_001730.1:n.460-314_460-310del
XM_011523309.2:c.460-314_460-310del	XP_011521611.1:n.460-314_460-310del
XM_017023646.1:c.460-314_460-310del	XP_016879135.1:n.460-314_460-310del
XM_024450434.1:c.82-314_82-310del	XP_024306202.1:n.82-314_82-310del
XR_002957839.1:n.585-314_585-310del
NM_001367225.1:c.460-314_460-310del	NP_001354154.1:n.460-314_460-310del
NR_159798.1:n.539-314_539-310del
NR_159799.1:n.420-314_420-310del