Linked Data
ClinVar Variation Id:
3223664
ClinVar RCV Id:
RCV004516428
MyVariant Identifiers:
chrX:g.31792101G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31773984G>A , CM000685.2:g.31773984G>A | GRCh38 |
| NC_000023.10:g.31792101G>A , CM000685.1:g.31792101G>A | GRCh37 |
| NC_000023.9:g.31702022G>A | NCBI36 |
| NG_012232.1:g.1570626C>T , LRG_199:g.1570626C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.2364C>T | ENSP00000350765.3:p.Ile788= | |
| ENST00000682238.1:c.138C>T | ENSP00000508124.1:p.Ile46= | |
| ENST00000683117.1:n.1179C>T | ||
| ENST00000683450.1:n.1101C>T | ||
| ENST00000683851.1:n.1179C>T | ||
| ENST00000683957.1:n.1010C>T | ||
| ENST00000684130.1:c.138C>T | ENSP00000508037.1:p.Ile46= | |
| ENST00000357033.9:c.7518C>T MANE Select | ENSP00000354923.3:p.Ile2506= | |
| ENST00000619831.5:c.3486C>T | ENSP00000479270.2:p.Ile1162= | |
| ENST00000620040.5:c.138C>T | ENSP00000478150.2:p.Ile46= | |
| ENST00000680961.1:c.138C>T | ENSP00000506386.1:p.Ile46= | |
| ENST00000681646.1:n.1179C>T | ||
| ENST00000681839.1:c.507C>T | ENSP00000505228.1:p.Ile169= | |
| ENST00000357033.8:c.7518C>T | ENSP00000354923.3:p.Ile2506= | |
| ENST00000358062.6:c.606C>T | ENSP00000350765.2:p.Ile202= | |
| ENST00000359836.5:c.138C>T | ENSP00000352894.1:p.Ile46= | |
| ENST00000378677.6:c.7506C>T | ENSP00000367948.2:p.Ile2502= | |
| ENST00000378707.7:c.138C>T | ENSP00000367979.3:p.Ile46= | |
| ENST00000471779.1:c.275C>T | ENSP00000417075.1:n.275C>T | |
| ENST00000474231.5:c.138C>T | ENSP00000417123.1:p.Ile46= | |
| ENST00000541735.5:c.138C>T | ENSP00000444119.1:p.Ile46= | |
| ENST00000619831.4:c.7503C>T | ENSP00000479270.1:p.Ile2501= | |
| ENST00000620040.4:c.7515C>T | ENSP00000478150.1:p.Ile2505= | |
| NM_000109.3:c.7494C>T | NP_000100.2:p.Ile2498= | |
| NM_004006.2:c.7518C>T , LRG_199t1:c.7518C>T | NP_003997.1:p.Ile2506= | |
| NM_004009.3:c.7506C>T | NP_004000.1:p.Ile2502= | |
| NM_004010.3:c.7149C>T | NP_004001.1:p.Ile2383= | |
| NM_004011.3:c.3495C>T | NP_004002.2:p.Ile1165= | |
| NM_004012.3:c.3486C>T | NP_004003.1:p.Ile1162= | |
| NM_004013.2:c.138C>T | NP_004004.1:p.Ile46= | |
| NM_004020.3:c.138C>T | NP_004011.2:p.Ile46= | |
| NM_004021.2:c.138C>T | NP_004012.1:p.Ile46= | |
| NM_004022.2:c.138C>T | NP_004013.1:p.Ile46= | |
| NM_004023.2:c.138C>T | NP_004014.1:p.Ile46= | |
| XM_006724468.2:c.7518C>T | XP_006724531.1:p.Ile2506= | |
| XM_006724469.2:c.7494C>T | XP_006724532.1:p.Ile2498= | |
| XM_006724470.2:c.7518C>T | XP_006724533.1:p.Ile2506= | |
| XM_006724471.2:c.7518C>T | XP_006724534.1:p.Ile2506= | |
| XM_006724472.2:c.7389C>T | XP_006724535.1:p.Ile2463= | |
| XM_006724473.2:c.7380C>T | XP_006724536.1:p.Ile2460= | |
| XM_006724474.2:c.7518C>T | XP_006724537.1:p.Ile2506= | |
| XM_006724475.2:c.7518C>T | XP_006724538.1:p.Ile2506= | |
| XM_011545467.1:c.7395C>T | XP_011543769.1:p.Ile2465= | |
| XM_011545468.1:c.7518C>T | XP_011543770.1:p.Ile2506= | |
| XM_006724469.3:c.7494C>T | XP_006724532.1:p.Ile2498= | |
| XM_006724470.3:c.7518C>T | XP_006724533.1:p.Ile2506= | |
| XM_006724474.3:c.7518C>T | XP_006724537.1:p.Ile2506= | |
| XM_011545468.2:c.7518C>T | XP_011543770.1:p.Ile2506= | |
| XM_017029328.1:c.7518C>T | XP_016884817.1:p.Ile2506= | |
| XM_017029331.1:c.1692C>T | XP_016884820.1:p.Ile564= | |
| NM_000109.4:c.7494C>T | NP_000100.3:p.Ile2498= | |
| NM_004006.3:c.7518C>T MANE Select | NP_003997.2:p.Ile2506= | |
| NM_004011.4:c.3495C>T | NP_004002.3:p.Ile1165= | |
| NM_004012.4:c.3486C>T | NP_004003.2:p.Ile1162= | |
| NM_004021.3:c.138C>T | NP_004012.2:p.Ile46= | |
| NM_004023.3:c.138C>T | NP_004014.2:p.Ile46= | |
| NM_004013.3:c.138C>T | NP_004004.2:p.Ile46= | |
| NM_004020.4:c.138C>T | NP_004011.3:p.Ile46= | |
| NM_004022.3:c.138C>T | NP_004013.2:p.Ile46= |