Canonical Allele Identifier: CA624156124
Gene: CA5A HGNC NCBI

Linked Data

dbSNP Id: rs1351450845

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902738_87902739del , CM000678.2:g.87902738_87902739del GRCh38
NC_000016.9:g.87936344_87936345del , CM000678.1:g.87936344_87936345del GRCh37
NC_000016.8:g.86493845_86493846del NCBI36
NG_033227.1:g.38771_38772del
NG_033227.2:g.38794_38795del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648022.1:c.460-216_460-215del ENSP00000497934.1:n.460-216_460-215del
ENST00000648177.1:c.341-216_341-215del ENSP00000497626.1:n.341-216_341-215del
ENST00000649158.1:c.460-216_460-215del ENSP00000496993.1:n.460-216_460-215del
ENST00000649794.3:c.460-216_460-215del MANE Select ENSP00000498065.2:n.460-216_460-215del
ENST00000309893.3:c.460-216_460-215del ENSP00000309649.2:n.460-216_460-215del
NM_001739.1:c.460-216_460-215del NP_001730.1:n.460-216_460-215del
XM_011523309.1:c.460-216_460-215del XP_011521611.1:n.460-216_460-215del
XM_011523310.1:c.460-216_460-215del XP_011521612.1:n.460-216_460-215del
XR_933417.1:n.579-216_579-215del
NM_001739.2:c.460-216_460-215del MANE Select NP_001730.1:n.460-216_460-215del
XM_011523309.2:c.460-216_460-215del XP_011521611.1:n.460-216_460-215del
XM_017023646.1:c.460-216_460-215del XP_016879135.1:n.460-216_460-215del
XM_024450434.1:c.82-216_82-215del XP_024306202.1:n.82-216_82-215del
XR_002957839.1:n.585-216_585-215del
NM_001367225.1:c.460-216_460-215del NP_001354154.1:n.460-216_460-215del
NR_159798.1:n.539-216_539-215del
NR_159799.1:n.420-216_420-215del