Canonical Allele Identifier: CA919764158
Gene: CA5A HGNC NCBI

Linked Data

dbSNP Id: rs35068596

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902756_87902762del , CM000678.2:g.87902756_87902762del GRCh38
NC_000016.9:g.87936362_87936368del , CM000678.1:g.87936362_87936368del GRCh37
NC_000016.8:g.86493863_86493869del NCBI36
NG_033227.1:g.38750_38756del
NG_033227.2:g.38773_38779del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648022.1:c.460-237_460-231del ENSP00000497934.1:n.460-237_460-231del
ENST00000648177.1:c.341-237_341-231del ENSP00000497626.1:n.341-237_341-231del
ENST00000649158.1:c.460-237_460-231del ENSP00000496993.1:n.460-237_460-231del
ENST00000649794.3:c.460-237_460-231del MANE Select ENSP00000498065.2:n.460-237_460-231del
ENST00000309893.3:c.460-237_460-231del ENSP00000309649.2:n.460-237_460-231del
NM_001739.1:c.460-237_460-231del NP_001730.1:n.460-237_460-231del
XM_011523309.1:c.460-237_460-231del XP_011521611.1:n.460-237_460-231del
XM_011523310.1:c.460-237_460-231del XP_011521612.1:n.460-237_460-231del
XR_933417.1:n.579-237_579-231del
NM_001739.2:c.460-237_460-231del MANE Select NP_001730.1:n.460-237_460-231del
XM_011523309.2:c.460-237_460-231del XP_011521611.1:n.460-237_460-231del
XM_017023646.1:c.460-237_460-231del XP_016879135.1:n.460-237_460-231del
XM_024450434.1:c.82-237_82-231del XP_024306202.1:n.82-237_82-231del
XR_002957839.1:n.585-237_585-231del
NM_001367225.1:c.460-237_460-231del NP_001354154.1:n.460-237_460-231del
NR_159798.1:n.539-237_539-231del
NR_159799.1:n.420-237_420-231del