Canonical Allele Identifier: CA2634808006
Gene: CA5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87902621_87902622insTT , CM000678.2:g.87902621_87902622insTT GRCh38
NC_000016.9:g.87936227_87936228insTT , CM000678.1:g.87936227_87936228insTT GRCh37
NC_000016.8:g.86493728_86493729insTT NCBI36
NG_033227.1:g.38885_38886insAA
NG_033227.2:g.38908_38909insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648022.1:c.460-102_460-101insAA ENSP00000497934.1:n.460-102_460-101insAA
ENST00000648177.1:c.341-102_341-101insAA ENSP00000497626.1:n.341-102_341-101insAA
ENST00000649158.1:c.460-102_460-101insAA ENSP00000496993.1:n.460-102_460-101insAA
ENST00000649794.3:c.460-102_460-101insAA MANE Select ENSP00000498065.2:n.460-102_460-101insAA
ENST00000309893.3:c.460-102_460-101insAA ENSP00000309649.2:n.460-102_460-101insAA
NM_001739.1:c.460-102_460-101insAA NP_001730.1:n.460-102_460-101insAA
XM_011523309.1:c.460-102_460-101insAA XP_011521611.1:n.460-102_460-101insAA
XM_011523310.1:c.460-102_460-101insAA XP_011521612.1:n.460-102_460-101insAA
XR_933417.1:n.579-102_579-101insAA
NM_001739.2:c.460-102_460-101insAA MANE Select NP_001730.1:n.460-102_460-101insAA
XM_011523309.2:c.460-102_460-101insAA XP_011521611.1:n.460-102_460-101insAA
XM_017023646.1:c.460-102_460-101insAA XP_016879135.1:n.460-102_460-101insAA
XM_024450434.1:c.82-102_82-101insAA XP_024306202.1:n.82-102_82-101insAA
XR_002957839.1:n.585-102_585-101insAA
NM_001367225.1:c.460-102_460-101insAA NP_001354154.1:n.460-102_460-101insAA
NR_159798.1:n.539-102_539-101insAA
NR_159799.1:n.420-102_420-101insAA