Canonical Allele Identifier: CA2240759119

Gene: CA5A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902364_87902365delinsAG , CM000678.2:g.87902364_87902365delinsAG	GRCh38
NC_000016.9:g.87935970_87935971delinsAG , CM000678.1:g.87935970_87935971delinsAG	GRCh37
NC_000016.8:g.86493471_86493472delinsAG	NCBI36
NG_033227.1:g.39142_39143delinsCT
NG_033227.2:g.39165_39166delinsCT

Transcript Alleles

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