Canonical Allele Identifier: CA2240759280

Gene: CA5A

Linked Data

• dbSNP Id: rs2055895628

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902674_87902679del , CM000678.2:g.87902674_87902679del	GRCh38
NC_000016.9:g.87936280_87936285del , CM000678.1:g.87936280_87936285del	GRCh37
NC_000016.8:g.86493781_86493786del	NCBI36
NG_033227.1:g.38836_38841del
NG_033227.2:g.38859_38864del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.460-151_460-146del	ENSP00000497934.1:n.460-151_460-146del
ENST00000648177.1:c.341-151_341-146del	ENSP00000497626.1:n.341-151_341-146del
ENST00000649158.1:c.460-151_460-146del	ENSP00000496993.1:n.460-151_460-146del
ENST00000649794.3:c.460-151_460-146del MANE Select	ENSP00000498065.2:n.460-151_460-146del
ENST00000309893.3:c.460-151_460-146del	ENSP00000309649.2:n.460-151_460-146del
NM_001739.1:c.460-151_460-146del	NP_001730.1:n.460-151_460-146del
XM_011523309.1:c.460-151_460-146del	XP_011521611.1:n.460-151_460-146del
XM_011523310.1:c.460-151_460-146del	XP_011521612.1:n.460-151_460-146del
XR_933417.1:n.579-151_579-146del
NM_001739.2:c.460-151_460-146del MANE Select	NP_001730.1:n.460-151_460-146del
XM_011523309.2:c.460-151_460-146del	XP_011521611.1:n.460-151_460-146del
XM_017023646.1:c.460-151_460-146del	XP_016879135.1:n.460-151_460-146del
XM_024450434.1:c.82-151_82-146del	XP_024306202.1:n.82-151_82-146del
XR_002957839.1:n.585-151_585-146del
NM_001367225.1:c.460-151_460-146del	NP_001354154.1:n.460-151_460-146del
NR_159798.1:n.539-151_539-146del
NR_159799.1:n.420-151_420-146del