Linked Data
ClinVar Variation Id:
222141
dbSNP Id:
rs111422676
ExAC:
X:100652999 C / T
gnomAD v2:
X-100652999-C-T
gnomAD v3:
X-101398011-C-T
gnomAD v4:
X-101398011-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101398011C>T , CM000685.2:g.101398011C>T | GRCh38 |
| NC_000023.10:g.100652999C>T , CM000685.1:g.100652999C>T | GRCh37 |
| NC_000023.9:g.100539655C>T | NCBI36 |
| NG_007119.1:g.14953G>A , LRG_672:g.14953G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000486121.7:c.*534G>A (GLA) | ENSP00000501124.2:n.*534G>A | |
| ENST00000674127.2:c.*591G>A (GLA) | ENSP00000501044.2:n.*591G>A | |
| ENST00000710365.1:c.1163G>A (GLA) | ENSP00000518234.1:p.Arg388His | |
| ENST00000218516.4:c.1088G>A (GLA) MANE Select | ENSP00000218516.4:p.Arg363His | |
| ENST00000466414.2:n.1224G>A (GLA) | ||
| ENST00000468823.2:n.2510G>A (GLA) | ||
| ENST00000479445.2:n.1702G>A (GLA) | ||
| ENST00000480513.6:c.*396G>A (GLA) | ENSP00000497055.1:n.*396G>A | |
| ENST00000486121.6:c.1133G>A (GLA) | ||
| ENST00000649178.1:c.1211G>A (GLA) | ENSP00000498186.1:p.Arg404His | |
| ENST00000674127.1:c.1188G>A (GLA) | ENSP00000501044.1:n.1188G>A | |
| ENST00000674142.1:n.1392G>A (GLA) | ||
| ENST00000675592.1:c.890G>A (GLA) | ENSP00000502239.1:p.Arg297His | |
| ENST00000675799.1:c.*613G>A (GLA) | ENSP00000502661.1:n.*613G>A | |
| ENST00000675968.1:n.3959G>A (GLA) | ||
| ENST00000676156.1:c.1052G>A (GLA) | ENSP00000501730.1:p.Arg351His | |
| ENST00000676372.1:c.1154G>A (GLA) | ENSP00000502805.1:n.1154G>A | |
| ENST00000218516.3:c.1088G>A (GLA) | ENSP00000218516.3:p.Arg363His | |
| ENST00000409170.3:c.300+2554C>T (RPL36A-HNRNPH2) | ENSP00000386655.4:n.300+2554C>T | |
| ENST00000409338.5:c.177+6189C>T (RPL36A-HNRNPH2) | ENSP00000386974.2:n.177+6189C>T | |
| ENST00000466414.1:n.414G>A (GLA) | ||
| ENST00000493905.6:c.*476G>A (GLA) | ENSP00000476935.1:n.*476G>A | |
| NM_000169.2:c.1088G>A , LRG_672t1:c.1088G>A (GLA) | NP_000160.1:p.Arg363His | |
| NM_001199973.1:c.408+2554C>T (RPL36A-HNRNPH2) | NP_001186902.1:n.408+2554C>T | |
| NM_001199974.1:c.285+6189C>T (RPL36A-HNRNPH2) | NP_001186903.1:n.285+6189C>T | |
| XR_938397.1:n.1173G>A (GLA) | ||
| XR_938397.2:n.1194G>A (GLA) | ||
| NM_001199973.2:c.300+2554C>T (RPL36A-HNRNPH2) | NP_001186902.2:n.300+2554C>T | |
| NM_001199974.2:c.177+6189C>T (RPL36A-HNRNPH2) | NP_001186903.2:n.177+6189C>T | |
| NM_000169.3:c.1088G>A (GLA) MANE Select | NP_000160.1:p.Arg363His | |
| NR_164783.1:n.1167G>A (GLA) |