Canonical Allele Identifier: CA2634807167

Gene: CA5A

Linked Data

• gnomAD v4: 16-87902359-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902359_87902360insG , CM000678.2:g.87902359_87902360insG	GRCh38
NC_000016.9:g.87935965_87935966insG , CM000678.1:g.87935965_87935966insG	GRCh37
NC_000016.8:g.86493466_86493467insG	NCBI36
NG_033227.1:g.39147_39148insC
NG_033227.2:g.39170_39171insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.555+65_555+66insC	ENSP00000497934.1:n.555+65_555+66insC
ENST00000648177.1:c.436+65_436+66insC	ENSP00000497626.1:n.436+65_436+66insC
ENST00000649158.1:c.555+65_555+66insC	ENSP00000496993.1:n.555+65_555+66insC
ENST00000649794.3:c.555+65_555+66insC MANE Select	ENSP00000498065.2:n.555+65_555+66insC
ENST00000309893.3:c.555+65_555+66insC	ENSP00000309649.2:n.555+65_555+66insC
NM_001739.1:c.555+65_555+66insC	NP_001730.1:n.555+65_555+66insC
XM_011523309.1:c.555+65_555+66insC	XP_011521611.1:n.555+65_555+66insC
XM_011523310.1:c.555+65_555+66insC	XP_011521612.1:n.555+65_555+66insC
XR_933417.1:n.674+65_674+66insC
NM_001739.2:c.555+65_555+66insC MANE Select	NP_001730.1:n.555+65_555+66insC
XM_011523309.2:c.555+65_555+66insC	XP_011521611.1:n.555+65_555+66insC
XM_017023646.1:c.555+65_555+66insC	XP_016879135.1:n.555+65_555+66insC
XM_024450434.1:c.177+65_177+66insC	XP_024306202.1:n.177+65_177+66insC
XR_002957839.1:n.680+65_680+66insC
NM_001367225.1:c.555+65_555+66insC	NP_001354154.1:n.555+65_555+66insC
NR_159798.1:n.634+65_634+66insC
NR_159799.1:n.515+65_515+66insC