Canonical Allele Identifier: CA980253815

Gene: CA5A

Linked Data

• dbSNP Id: rs2055898396
• gnomAD v3: 16-87902768-TG-T
• gnomAD v4: 16-87902768-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902771del , CM000678.2:g.87902771del	GRCh38
NC_000016.9:g.87936377del , CM000678.1:g.87936377del	GRCh37
NC_000016.8:g.86493878del	NCBI36
NG_033227.1:g.38738del
NG_033227.2:g.38761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.460-249del	ENSP00000497934.1:n.460-249del
ENST00000648177.1:c.341-249del	ENSP00000497626.1:n.341-249del
ENST00000649158.1:c.460-249del	ENSP00000496993.1:n.460-249del
ENST00000649794.3:c.460-249del MANE Select	ENSP00000498065.2:n.460-249del
ENST00000309893.3:c.460-249del	ENSP00000309649.2:n.460-249del
NM_001739.1:c.460-249del	NP_001730.1:n.460-249del
XM_011523309.1:c.460-249del	XP_011521611.1:n.460-249del
XM_011523310.1:c.460-249del	XP_011521612.1:n.460-249del
XR_933417.1:n.579-249del
NM_001739.2:c.460-249del MANE Select	NP_001730.1:n.460-249del
XM_011523309.2:c.460-249del	XP_011521611.1:n.460-249del
XM_017023646.1:c.460-249del	XP_016879135.1:n.460-249del
XM_024450434.1:c.82-249del	XP_024306202.1:n.82-249del
XR_002957839.1:n.585-249del
NM_001367225.1:c.460-249del	NP_001354154.1:n.460-249del
NR_159798.1:n.539-249del
NR_159799.1:n.420-249del