Canonical Allele Identifier: CA2240759129
Gene: CA5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902380_87902382delinsGAT , CM000678.2:g.87902380_87902382delinsGAT GRCh38
NC_000016.9:g.87935986_87935988delinsGAT , CM000678.1:g.87935986_87935988delinsGAT GRCh37
NC_000016.8:g.86493487_86493489delinsGAT NCBI36
NG_033227.1:g.39125_39127delinsATC
NG_033227.2:g.39148_39150delinsATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648022.1:c.555+43_555+45delinsATC ENSP00000497934.1:n.555+43_555+45delinsATC
ENST00000648177.1:c.436+43_436+45delinsATC ENSP00000497626.1:n.436+43_436+45delinsATC
ENST00000649158.1:c.555+43_555+45delinsATC ENSP00000496993.1:n.555+43_555+45delinsATC
ENST00000649794.3:c.555+43_555+45delinsATC MANE Select ENSP00000498065.2:n.555+43_555+45delinsATC
ENST00000309893.3:c.555+43_555+45delinsATC ENSP00000309649.2:n.555+43_555+45delinsATC
NM_001739.1:c.555+43_555+45delinsATC NP_001730.1:n.555+43_555+45delinsATC
XM_011523309.1:c.555+43_555+45delinsATC XP_011521611.1:n.555+43_555+45delinsATC
XM_011523310.1:c.555+43_555+45delinsATC XP_011521612.1:n.555+43_555+45delinsATC
XR_933417.1:n.674+43_674+45delinsATC
NM_001739.2:c.555+43_555+45delinsATC MANE Select NP_001730.1:n.555+43_555+45delinsATC
XM_011523309.2:c.555+43_555+45delinsATC XP_011521611.1:n.555+43_555+45delinsATC
XM_017023646.1:c.555+43_555+45delinsATC XP_016879135.1:n.555+43_555+45delinsATC
XM_024450434.1:c.177+43_177+45delinsATC XP_024306202.1:n.177+43_177+45delinsATC
XR_002957839.1:n.680+43_680+45delinsATC
NM_001367225.1:c.555+43_555+45delinsATC NP_001354154.1:n.555+43_555+45delinsATC
NR_159798.1:n.634+43_634+45delinsATC
NR_159799.1:n.515+43_515+45delinsATC