Canonical Allele Identifier: CA2634807180

Gene: CA5A

Linked Data

• gnomAD v4: 16-87902364-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902364_87902365insT , CM000678.2:g.87902364_87902365insT	GRCh38
NC_000016.9:g.87935970_87935971insT , CM000678.1:g.87935970_87935971insT	GRCh37
NC_000016.8:g.86493471_86493472insT	NCBI36
NG_033227.1:g.39142_39143insA
NG_033227.2:g.39165_39166insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.555+60_555+61insA	ENSP00000497934.1:n.555+60_555+61insA
ENST00000648177.1:c.436+60_436+61insA	ENSP00000497626.1:n.436+60_436+61insA
ENST00000649158.1:c.555+60_555+61insA	ENSP00000496993.1:n.555+60_555+61insA
ENST00000649794.3:c.555+60_555+61insA MANE Select	ENSP00000498065.2:n.555+60_555+61insA
ENST00000309893.3:c.555+60_555+61insA	ENSP00000309649.2:n.555+60_555+61insA
NM_001739.1:c.555+60_555+61insA	NP_001730.1:n.555+60_555+61insA
XM_011523309.1:c.555+60_555+61insA	XP_011521611.1:n.555+60_555+61insA
XM_011523310.1:c.555+60_555+61insA	XP_011521612.1:n.555+60_555+61insA
XR_933417.1:n.674+60_674+61insA
NM_001739.2:c.555+60_555+61insA MANE Select	NP_001730.1:n.555+60_555+61insA
XM_011523309.2:c.555+60_555+61insA	XP_011521611.1:n.555+60_555+61insA
XM_017023646.1:c.555+60_555+61insA	XP_016879135.1:n.555+60_555+61insA
XM_024450434.1:c.177+60_177+61insA	XP_024306202.1:n.177+60_177+61insA
XR_002957839.1:n.680+60_680+61insA
NM_001367225.1:c.555+60_555+61insA	NP_001354154.1:n.555+60_555+61insA
NR_159798.1:n.634+60_634+61insA
NR_159799.1:n.515+60_515+61insA