Canonical Allele Identifier: CA980253683

Gene: CA5A

Linked Data

• gnomAD v3: 16-87902376-G-GAC
• gnomAD v4: 16-87902376-G-GAC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902377_87902378insCA , CM000678.2:g.87902377_87902378insCA	GRCh38
NC_000016.9:g.87935983_87935984insCA , CM000678.1:g.87935983_87935984insCA	GRCh37
NC_000016.8:g.86493484_86493485insCA	NCBI36
NG_033227.1:g.39130_39131insGT
NG_033227.2:g.39153_39154insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.555+48_555+49insGT	ENSP00000497934.1:n.555+48_555+49insGT
ENST00000648177.1:c.436+48_436+49insGT	ENSP00000497626.1:n.436+48_436+49insGT
ENST00000649158.1:c.555+48_555+49insGT	ENSP00000496993.1:n.555+48_555+49insGT
ENST00000649794.3:c.555+48_555+49insGT MANE Select	ENSP00000498065.2:n.555+48_555+49insGT
ENST00000309893.3:c.555+48_555+49insGT	ENSP00000309649.2:n.555+48_555+49insGT
NM_001739.1:c.555+48_555+49insGT	NP_001730.1:n.555+48_555+49insGT
XM_011523309.1:c.555+48_555+49insGT	XP_011521611.1:n.555+48_555+49insGT
XM_011523310.1:c.555+48_555+49insGT	XP_011521612.1:n.555+48_555+49insGT
XR_933417.1:n.674+48_674+49insGT
NM_001739.2:c.555+48_555+49insGT MANE Select	NP_001730.1:n.555+48_555+49insGT
XM_011523309.2:c.555+48_555+49insGT	XP_011521611.1:n.555+48_555+49insGT
XM_017023646.1:c.555+48_555+49insGT	XP_016879135.1:n.555+48_555+49insGT
XM_024450434.1:c.177+48_177+49insGT	XP_024306202.1:n.177+48_177+49insGT
XR_002957839.1:n.680+48_680+49insGT
NM_001367225.1:c.555+48_555+49insGT	NP_001354154.1:n.555+48_555+49insGT
NR_159798.1:n.634+48_634+49insGT
NR_159799.1:n.515+48_515+49insGT