Linked Data
ClinVar Variation Id:
68362
dbSNP Id:
rs199474784
ExAC:
17:29670033 G / A
gnomAD v2:
17-29670033-G-A
gnomAD v4:
17-31343015-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.31343015G>A , CM000679.2:g.31343015G>A | GRCh38 |
| NC_000017.10:g.29670033G>A , CM000679.1:g.29670033G>A | GRCh37 |
| NC_000017.9:g.26694159G>A | NCBI36 |
| NG_009018.1:g.253039G>A , LRG_214:g.253039G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696138.1:c.7051G>A | ENSP00000512431.1:p.Glu2351Lys | |
| ENST00000684826.1:c.1633G>A | ENSP00000509994.1:p.Glu545Lys | |
| ENST00000687027.1:c.1225G>A | ENSP00000508715.1:p.Glu409Lys | |
| ENST00000687863.1:n.3714G>A | ||
| ENST00000689464.1:c.8G>A | ||
| ENST00000691014.1:c.7099G>A | ENSP00000510595.1:p.Glu2367Lys | |
| ENST00000693617.1:c.1633G>A | ENSP00000510031.1:p.Glu545Lys | |
| ENST00000358273.9:c.7069G>A MANE Select | ENSP00000351015.4:p.Glu2357Lys | |
| ENST00000356175.7:c.7006G>A | ENSP00000348498.3:p.Glu2336Lys | |
| ENST00000358273.8:c.7069G>A | ENSP00000351015.4:p.Glu2357Lys | |
| ENST00000456735.6:c.6004G>A | ENSP00000389907.2:p.Glu2002Lys | |
| ENST00000471572.6:c.452G>A | ||
| ENST00000579081.5:c.7205G>A | ENSP00000462408.1:n.7205G>A | |
| ENST00000581790.5:c.212G>A | ||
| ENST00000582892.1:n.311G>A | ||
| ENST00000584328.1:n.483G>A | ||
| NM_000267.3:c.7006G>A , LRG_214t1:c.7006G>A | NP_000258.1:p.Glu2336Lys | |
| NM_001042492.2:c.7069G>A , LRG_214t2:c.7069G>A | NP_001035957.1:p.Glu2357Lys | |
| XM_005257983.1:c.7069G>A | XP_005258040.1:p.Glu2357Lys | |
| XM_005257984.1:c.7006G>A | XP_005258041.1:p.Glu2336Lys | |
| XM_006721922.1:c.7099G>A | XP_006721985.1:p.Glu2367Lys | |
| XM_006721923.2:c.7060G>A | XP_006721986.1:p.Glu2354Lys | |
| XM_006721924.1:c.7099G>A | XP_006721987.1:p.Glu2367Lys | |
| XM_006721925.1:c.7036G>A | XP_006721988.1:p.Glu2346Lys | |
| XM_006721926.2:c.7099G>A | XP_006721989.1:p.Glu2367Lys | |
| XM_006721927.1:c.7099G>A | XP_006721990.1:p.Glu2367Lys | |
| XM_011524852.1:c.7096G>A | XP_011523154.1:p.Glu2366Lys | |
| XM_011524853.1:c.7060G>A | XP_011523155.1:p.Glu2354Lys | |
| XM_011524854.1:c.7060G>A | XP_011523156.1:p.Glu2354Lys | |
| XM_011524855.1:c.7060G>A | XP_011523157.1:p.Glu2354Lys | |
| XM_011524856.1:c.7060G>A | XP_011523158.1:p.Glu2354Lys | |
| XM_011524857.1:c.7099G>A | XP_011523159.1:p.Glu2367Lys | |
| NM_001042492.3:c.7069G>A MANE Select | NP_001035957.1:p.Glu2357Lys |