OUTAGE/INTERRUPTION NOTICE:2024-06-14T21:00:00-0400 — 2024-06-17T08:00:00-0400
The first of two essential broad service outages will occur over the weekend.
The outage is expected to be shorter than the indicated time, but due to its scope and importance, a longer window is planned.
Affected ClinGen services include the UIs and APIs of the Allele Registry, ACI, Cspec, Erepo, LDH
The first of two essential broad service outages will occur over the weekend.
The outage is expected to be shorter than the indicated time, but due to its scope and importance, a longer window is planned.
Affected ClinGen services include the UIs and APIs of the Allele Registry, ACI, Cspec, Erepo, LDH
Linked Data
ClinVar Variation Id:
2966765
ClinVar RCV Id:
RCV003828899
dbSNP Id:
rs1752485593
gnomAD v4:
5-132385341-T-A
MyVariant Identifiers:
chr5:g.131721033T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132385341T>A , CM000667.2:g.132385341T>A | GRCh38 |
| NC_000005.9:g.131721033T>A , CM000667.1:g.131721033T>A | GRCh37 |
| NC_000005.8:g.131748932T>A | NCBI36 |
| NG_008982.1:g.20633T>A | |
| NG_008982.2:g.20638T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415928.6:c.665+1027T>A | ENSP00000388838.2:n.665+1027T>A | |
| ENST00000435065.7:c.738T>A | ENSP00000402760.2:p.Leu246= | |
| ENST00000448810.6:c.666T>A | ENSP00000401860.2:p.Leu222= | |
| ENST00000686757.1:c.685T>A | ENSP00000510721.1:p.Trp229Arg | |
| ENST00000687740.1:n.1826T>A | ||
| ENST00000688151.1:n.1858T>A | ||
| ENST00000689271.1:c.671+1021T>A | ENSP00000510797.1:n.671+1021T>A | |
| ENST00000690900.1:c.672-35T>A | ENSP00000510703.1:n.672-35T>A | |
| ENST00000692212.1:n.492T>A | ||
| ENST00000692355.1:c.204+1040T>A | ||
| ENST00000692413.1:c.685T>A | ENSP00000509374.1:p.Trp229Arg | |
| ENST00000692825.1:c.734T>A | ENSP00000509447.1:n.734T>A | |
| ENST00000693308.1:c.679T>A | ENSP00000509770.1:p.Trp227Arg | |
| ENST00000693763.1:n.1826T>A | ||
| ENST00000245407.8:c.666T>A MANE Select | ENSP00000245407.3:p.Leu222= | |
| ENST00000245407.7:c.666T>A | ENSP00000245407.3:p.Leu222= | |
| ENST00000415928.5:c.435T>A | ENSP00000388838.1:p.Leu145= | |
| ENST00000435065.6:c.738T>A | ENSP00000402760.2:p.Leu246= | |
| ENST00000437841.6:c.407T>A | ENSP00000400553.1:p.Leu136Ter | |
| ENST00000448810.5:c.14T>A | ||
| ENST00000461013.5:n.8088T>A | ||
| NM_001308122.1:c.738T>A | NP_001295051.1:p.Leu246= | |
| NM_003060.3:c.666T>A | NP_003051.1:p.Leu222= | |
| XM_011543590.1:c.48T>A | XP_011541892.1:p.Leu16= | |
| XR_427718.1:n.1026T>A | ||
| XR_948290.1:n.1007T>A | ||
| XR_948291.1:n.1020T>A | ||
| XM_011543590.2:c.48T>A | XP_011541892.1:p.Leu16= | |
| XM_017009778.2:c.138T>A | XP_016865267.1:p.Leu46= | |
| XR_001742215.1:n.1007T>A | ||
| XR_001742216.1:n.1026T>A | ||
| XR_427718.2:n.1026T>A | ||
| XR_948290.2:n.1007T>A | ||
| XR_948291.2:n.1020T>A | ||
| NM_003060.4:c.666T>A MANE Select | NP_003051.1:p.Leu222= | |
| NM_001308122.2:c.738T>A | NP_001295051.1:p.Leu246= |