Canonical Allele Identifier: CA624156061

Gene: CA5A

Linked Data

• dbSNP Id: rs1567520624
• gnomAD v2: 16-87936138-TGGAAAGA-T
• gnomAD v4: 16-87902532-TGGAAAGA-T
• MyVariant Identifiers: chr16:g.87936139_87936145del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902534_87902540del , CM000678.2:g.87902534_87902540del	GRCh38
NC_000016.9:g.87936140_87936146del , CM000678.1:g.87936140_87936146del	GRCh37
NC_000016.8:g.86493641_86493647del	NCBI36
NG_033227.1:g.38968_38974del
NG_033227.2:g.38991_38997del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.460-19_460-13del	ENSP00000497934.1:n.460-19_460-13del
ENST00000648177.1:c.341-19_341-13del	ENSP00000497626.1:n.341-19_341-13del
ENST00000649158.1:c.460-19_460-13del	ENSP00000496993.1:n.460-19_460-13del
ENST00000649794.3:c.460-19_460-13del MANE Select	ENSP00000498065.2:n.460-19_460-13del
ENST00000309893.3:c.460-19_460-13del	ENSP00000309649.2:n.460-19_460-13del
NM_001739.1:c.460-19_460-13del	NP_001730.1:n.460-19_460-13del
XM_011523309.1:c.460-19_460-13del	XP_011521611.1:n.460-19_460-13del
XM_011523310.1:c.460-19_460-13del	XP_011521612.1:n.460-19_460-13del
XR_933417.1:n.579-19_579-13del
NM_001739.2:c.460-19_460-13del MANE Select	NP_001730.1:n.460-19_460-13del
XM_011523309.2:c.460-19_460-13del	XP_011521611.1:n.460-19_460-13del
XM_017023646.1:c.460-19_460-13del	XP_016879135.1:n.460-19_460-13del
XM_024450434.1:c.82-19_82-13del	XP_024306202.1:n.82-19_82-13del
XR_002957839.1:n.585-19_585-13del
NM_001367225.1:c.460-19_460-13del	NP_001354154.1:n.460-19_460-13del
NR_159798.1:n.539-19_539-13del
NR_159799.1:n.420-19_420-13del