Canonical Allele Identifier: CA2634807147

Gene: CA5A

Linked Data

• gnomAD v4: 16-87902352-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902352_87902353insG , CM000678.2:g.87902352_87902353insG	GRCh38
NC_000016.9:g.87935958_87935959insG , CM000678.1:g.87935958_87935959insG	GRCh37
NC_000016.8:g.86493459_86493460insG	NCBI36
NG_033227.1:g.39154_39155insC
NG_033227.2:g.39177_39178insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.555+72_555+73insC	ENSP00000497934.1:n.555+72_555+73insC
ENST00000648177.1:c.436+72_436+73insC	ENSP00000497626.1:n.436+72_436+73insC
ENST00000649158.1:c.555+72_555+73insC	ENSP00000496993.1:n.555+72_555+73insC
ENST00000649794.3:c.555+72_555+73insC MANE Select	ENSP00000498065.2:n.555+72_555+73insC
ENST00000309893.3:c.555+72_555+73insC	ENSP00000309649.2:n.555+72_555+73insC
NM_001739.1:c.555+72_555+73insC	NP_001730.1:n.555+72_555+73insC
XM_011523309.1:c.555+72_555+73insC	XP_011521611.1:n.555+72_555+73insC
XM_011523310.1:c.555+72_555+73insC	XP_011521612.1:n.555+72_555+73insC
XR_933417.1:n.674+72_674+73insC
NM_001739.2:c.555+72_555+73insC MANE Select	NP_001730.1:n.555+72_555+73insC
XM_011523309.2:c.555+72_555+73insC	XP_011521611.1:n.555+72_555+73insC
XM_017023646.1:c.555+72_555+73insC	XP_016879135.1:n.555+72_555+73insC
XM_024450434.1:c.177+72_177+73insC	XP_024306202.1:n.177+72_177+73insC
XR_002957839.1:n.680+72_680+73insC
NM_001367225.1:c.555+72_555+73insC	NP_001354154.1:n.555+72_555+73insC
NR_159798.1:n.634+72_634+73insC
NR_159799.1:n.515+72_515+73insC