Linked Data
ClinVar Variation Id:
10737
ClinVar RCV Id:
RCV000011484
dbSNP Id:
rs28935489
PubMed:
PMID:7504405
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101398479G>A , CM000685.2:g.101398479G>A | GRCh38 |
| NC_000023.10:g.100653467G>A , CM000685.1:g.100653467G>A | GRCh37 |
| NC_000023.9:g.100540123G>A | NCBI36 |
| NG_007119.1:g.14485C>T , LRG_672:g.14485C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000486121.7:c.*336C>T (GLA) | ENSP00000501124.2:n.*336C>T | |
| ENST00000674127.2:c.*393C>T (GLA) | ENSP00000501044.2:n.*393C>T | |
| ENST00000710365.1:c.965C>T (GLA) | ENSP00000518234.1:p.Ser322Phe | |
| ENST00000218516.4:c.890C>T (GLA) MANE Select | ENSP00000218516.4:p.Ser297Phe | |
| ENST00000466414.2:n.1026C>T (GLA) | ||
| ENST00000468823.2:n.2042C>T (GLA) | ||
| ENST00000479445.2:n.1504C>T (GLA) | ||
| ENST00000480513.6:c.*198C>T (GLA) | ENSP00000497055.1:n.*198C>T | |
| ENST00000486121.6:c.935C>T (GLA) | ||
| ENST00000649178.1:c.1013C>T (GLA) | ENSP00000498186.1:p.Ser338Phe | |
| ENST00000674127.1:c.990C>T (GLA) | ENSP00000501044.1:n.990C>T | |
| ENST00000674142.1:n.1194C>T (GLA) | ||
| ENST00000674634.2:c.890C>T (GLA) | ENSP00000502629.2:p.Ser297Phe | |
| ENST00000675592.1:c.801+306C>T (GLA) | ENSP00000502239.1:n.801+306C>T | |
| ENST00000675799.1:c.*415C>T (GLA) | ENSP00000502661.1:n.*415C>T | |
| ENST00000675968.1:n.3761C>T (GLA) | ||
| ENST00000676156.1:c.854C>T (GLA) | ENSP00000501730.1:p.Ser285Phe | |
| ENST00000676372.1:c.956C>T (GLA) | ENSP00000502805.1:n.956C>T | |
| ENST00000218516.3:c.890C>T (GLA) | ENSP00000218516.3:p.Ser297Phe | |
| ENST00000409170.3:c.300+3022G>A (RPL36A-HNRNPH2) | ENSP00000386655.4:n.300+3022G>A | |
| ENST00000409338.5:c.177+6657G>A (RPL36A-HNRNPH2) | ENSP00000386974.2:n.177+6657G>A | |
| ENST00000466414.1:n.216C>T (GLA) | ||
| ENST00000493905.6:c.*278C>T (GLA) | ENSP00000476935.1:n.*278C>T | |
| NM_000169.2:c.890C>T , LRG_672t1:c.890C>T (GLA) | NP_000160.1:p.Ser297Phe | |
| NM_001199973.1:c.408+3022G>A (RPL36A-HNRNPH2) | NP_001186902.1:n.408+3022G>A | |
| NM_001199974.1:c.285+6657G>A (RPL36A-HNRNPH2) | NP_001186903.1:n.285+6657G>A | |
| XR_938397.1:n.975C>T (GLA) | ||
| XR_938397.2:n.996C>T (GLA) | ||
| NM_001199973.2:c.300+3022G>A (RPL36A-HNRNPH2) | NP_001186902.2:n.300+3022G>A | |
| NM_001199974.2:c.177+6657G>A (RPL36A-HNRNPH2) | NP_001186903.2:n.177+6657G>A | |
| NM_000169.3:c.890C>T (GLA) MANE Select | NP_000160.1:p.Ser297Phe | |
| NR_164783.1:n.969C>T (GLA) |