Canonical Allele Identifier: CA980253691

Gene: CA5A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902380_87902381insCG , CM000678.2:g.87902380_87902381insCG	GRCh38
NC_000016.9:g.87935986_87935987insCG , CM000678.1:g.87935986_87935987insCG	GRCh37
NC_000016.8:g.86493487_86493488insCG	NCBI36
NG_033227.1:g.39127_39128insGC
NG_033227.2:g.39150_39151insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.555+45_555+46insGC	ENSP00000497934.1:n.555+45_555+46insGC
ENST00000648177.1:c.436+45_436+46insGC	ENSP00000497626.1:n.436+45_436+46insGC
ENST00000649158.1:c.555+45_555+46insGC	ENSP00000496993.1:n.555+45_555+46insGC
ENST00000649794.3:c.555+45_555+46insGC MANE Select	ENSP00000498065.2:n.555+45_555+46insGC
ENST00000309893.3:c.555+45_555+46insGC	ENSP00000309649.2:n.555+45_555+46insGC
NM_001739.1:c.555+45_555+46insGC	NP_001730.1:n.555+45_555+46insGC
XM_011523309.1:c.555+45_555+46insGC	XP_011521611.1:n.555+45_555+46insGC
XM_011523310.1:c.555+45_555+46insGC	XP_011521612.1:n.555+45_555+46insGC
XR_933417.1:n.674+45_674+46insGC
NM_001739.2:c.555+45_555+46insGC MANE Select	NP_001730.1:n.555+45_555+46insGC
XM_011523309.2:c.555+45_555+46insGC	XP_011521611.1:n.555+45_555+46insGC
XM_017023646.1:c.555+45_555+46insGC	XP_016879135.1:n.555+45_555+46insGC
XM_024450434.1:c.177+45_177+46insGC	XP_024306202.1:n.177+45_177+46insGC
XR_002957839.1:n.680+45_680+46insGC
NM_001367225.1:c.555+45_555+46insGC	NP_001354154.1:n.555+45_555+46insGC
NR_159798.1:n.634+45_634+46insGC
NR_159799.1:n.515+45_515+46insGC