Canonical Allele Identifier: CA980253662
Gene: CA5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902362_87902364dup , CM000678.2:g.87902362_87902364dup GRCh38
NC_000016.9:g.87935968_87935970dup , CM000678.1:g.87935968_87935970dup GRCh37
NC_000016.8:g.86493469_86493471dup NCBI36
NG_033227.1:g.39152_39154dup
NG_033227.2:g.39175_39177dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000648022.1:c.555+70_555+72dup ENSP00000497934.1:n.555+70_555+72dup
ENST00000648177.1:c.436+70_436+72dup ENSP00000497626.1:n.436+70_436+72dup
ENST00000649158.1:c.555+70_555+72dup ENSP00000496993.1:n.555+70_555+72dup
ENST00000649794.3:c.555+70_555+72dup MANE Select ENSP00000498065.2:n.555+70_555+72dup
ENST00000309893.3:c.555+70_555+72dup ENSP00000309649.2:n.555+70_555+72dup
NM_001739.1:c.555+70_555+72dup NP_001730.1:n.555+70_555+72dup
XM_011523309.1:c.555+70_555+72dup XP_011521611.1:n.555+70_555+72dup
XM_011523310.1:c.555+70_555+72dup XP_011521612.1:n.555+70_555+72dup
XR_933417.1:n.674+70_674+72dup
NM_001739.2:c.555+70_555+72dup MANE Select NP_001730.1:n.555+70_555+72dup
XM_011523309.2:c.555+70_555+72dup XP_011521611.1:n.555+70_555+72dup
XM_017023646.1:c.555+70_555+72dup XP_016879135.1:n.555+70_555+72dup
XM_024450434.1:c.177+70_177+72dup XP_024306202.1:n.177+70_177+72dup
XR_002957839.1:n.680+70_680+72dup
NM_001367225.1:c.555+70_555+72dup NP_001354154.1:n.555+70_555+72dup
NR_159798.1:n.634+70_634+72dup
NR_159799.1:n.515+70_515+72dup