Canonical Allele Identifier: CA2634807336
Gene: CA5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902403_87902404dup , CM000678.2:g.87902403_87902404dup GRCh38
NC_000016.9:g.87936009_87936010dup , CM000678.1:g.87936009_87936010dup GRCh37
NC_000016.8:g.86493510_86493511dup NCBI36
NG_033227.1:g.39104_39105dup
NG_033227.2:g.39127_39128dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000648022.1:c.555+22_555+23dup ENSP00000497934.1:n.555+22_555+23dup
ENST00000648177.1:c.436+22_436+23dup ENSP00000497626.1:n.436+22_436+23dup
ENST00000649158.1:c.555+22_555+23dup ENSP00000496993.1:n.555+22_555+23dup
ENST00000649794.3:c.555+22_555+23dup MANE Select ENSP00000498065.2:n.555+22_555+23dup
ENST00000309893.3:c.555+22_555+23dup ENSP00000309649.2:n.555+22_555+23dup
NM_001739.1:c.555+22_555+23dup NP_001730.1:n.555+22_555+23dup
XM_011523309.1:c.555+22_555+23dup XP_011521611.1:n.555+22_555+23dup
XM_011523310.1:c.555+22_555+23dup XP_011521612.1:n.555+22_555+23dup
XR_933417.1:n.674+22_674+23dup
NM_001739.2:c.555+22_555+23dup MANE Select NP_001730.1:n.555+22_555+23dup
XM_011523309.2:c.555+22_555+23dup XP_011521611.1:n.555+22_555+23dup
XM_017023646.1:c.555+22_555+23dup XP_016879135.1:n.555+22_555+23dup
XM_024450434.1:c.177+22_177+23dup XP_024306202.1:n.177+22_177+23dup
XR_002957839.1:n.680+22_680+23dup
NM_001367225.1:c.555+22_555+23dup NP_001354154.1:n.555+22_555+23dup
NR_159798.1:n.634+22_634+23dup
NR_159799.1:n.515+22_515+23dup