Linked Data
ClinVar Variation Id:
37594
ClinVar RCV Id:
RCV000031175
RCV000240737
RCV000479398
RCV000458634
RCV000764128
RCV000219296
RCV001357250
RCV002267803
dbSNP Id:
rs397507233
ExAC:
17:41251893 T / G
gnomAD v2:
17-41251893-T-G
gnomAD v3:
17-43099876-T-G
gnomAD v4:
17-43099876-T-G
PubMed:
PMID:27257965
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43099876T>G , CM000679.2:g.43099876T>G | GRCh38 |
| NC_000017.10:g.41251893T>G , CM000679.1:g.41251893T>G | GRCh37 |
| NC_000017.9:g.38505419T>G | NCBI36 |
| NG_005905.2:g.118108A>C , LRG_292:g.118108A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.510A>C | ||
| ENST00000461574.2:c.446A>C | ENSP00000417241.2:p.Glu149Ala | |
| ENST00000470026.6:c.446A>C | ENSP00000419274.2:p.Glu149Ala | |
| ENST00000473961.6:c.443A>C | ENSP00000420201.2:p.Glu148Ala | |
| ENST00000476777.6:c.443A>C | ENSP00000417554.2:p.Glu148Ala | |
| ENST00000477152.6:c.368A>C | ENSP00000419988.2:p.Glu123Ala | |
| ENST00000478531.6:c.443A>C | ENSP00000420412.2:p.Glu148Ala | |
| ENST00000489037.2:c.368A>C | ENSP00000420781.2:p.Glu123Ala | |
| ENST00000493919.6:c.305A>C | ENSP00000418819.2:p.Glu102Ala | |
| ENST00000494123.6:c.446A>C | ENSP00000419103.2:p.Glu149Ala | |
| ENST00000497488.2:c.-218-5016A>C | ENSP00000418986.2:n.-218-5016A>C | |
| ENST00000618469.2:c.446A>C | ENSP00000478114.2:p.Glu149Ala | |
| ENST00000634433.2:c.446A>C | ENSP00000489431.2:p.Glu149Ala | |
| ENST00000644379.2:c.446A>C | ENSP00000496570.2:p.Glu149Ala | |
| ENST00000644555.2:c.305A>C | ENSP00000494614.2:p.Glu102Ala | |
| ENST00000652672.2:c.305A>C | ENSP00000498906.2:p.Glu102Ala | |
| ENST00000484087.6:c.446A>C | ENSP00000419481.2:p.Glu149Ala | |
| ENST00000700182.1:c.365A>C | ENSP00000514849.1:p.Glu122Ala | |
| ENST00000700183.1:c.*360A>C | ENSP00000514850.1:n.*360A>C | |
| ENST00000700184.1:n.686A>C | ||
| ENST00000357654.9:c.446A>C MANE Select | ENSP00000350283.3:p.Glu149Ala | |
| ENST00000471181.7:c.446A>C | ENSP00000418960.2:p.Glu149Ala | |
| ENST00000642945.1:c.*320A>C | ENSP00000495897.1:n.*320A>C | |
| ENST00000652672.1:c.305A>C | ENSP00000498906.1:p.Glu102Ala | |
| ENST00000352993.7:c.446A>C | ENSP00000312236.5:p.Glu149Ala | |
| ENST00000354071.7:c.446A>C | ENSP00000326002.7:p.Glu149Ala | |
| ENST00000357654.7:c.446A>C | ENSP00000350283.3:p.Glu149Ala | |
| ENST00000461221.5:c.*229A>C | ENSP00000418548.1:n.*229A>C | |
| ENST00000461798.5:c.*232A>C | ENSP00000417988.1:n.*232A>C | |
| ENST00000468300.5:c.446A>C | ENSP00000417148.1:p.Glu149Ala | |
| ENST00000470026.5:c.446A>C | ENSP00000419274.1:p.Glu149Ala | |
| ENST00000471181.6:c.446A>C | ENSP00000418960.2:p.Glu149Ala | |
| ENST00000473961.5:c.166A>C | ||
| ENST00000476777.5:c.443A>C | ENSP00000417554.1:p.Glu148Ala | |
| ENST00000477152.5:c.368A>C | ENSP00000419988.1:p.Glu123Ala | |
| ENST00000478531.5:c.443A>C | ENSP00000420412.1:p.Glu148Ala | |
| ENST00000484087.5:c.191A>C | ENSP00000419481.1:p.Glu64Ala | |
| ENST00000487825.5:c.194A>C | ENSP00000418212.1:p.Glu65Ala | |
| ENST00000491747.6:c.446A>C | ENSP00000420705.2:p.Glu149Ala | |
| ENST00000492859.5:c.*382A>C | ENSP00000420253.1:n.*382A>C | |
| ENST00000493795.5:c.305A>C | ENSP00000418775.1:p.Glu102Ala | |
| ENST00000493919.5:c.305A>C | ENSP00000418819.1:p.Glu102Ala | |
| ENST00000494123.5:c.446A>C | ENSP00000419103.1:p.Glu149Ala | |
| ENST00000497488.1:c.-218-5016A>C | ENSP00000418986.1:n.-218-5016A>C | |
| ENST00000586385.5:c.4+25306A>C | ENSP00000465818.1:n.4+25306A>C | |
| ENST00000591534.5:c.-43-25355A>C | ENSP00000467329.1:n.-43-25355A>C | |
| ENST00000591849.5:c.-99+25395A>C | ENSP00000465347.1:n.-99+25395A>C | |
| ENST00000634433.1:c.446A>C | ENSP00000489431.1:p.Glu149Ala | |
| NM_007294.3:c.446A>C , LRG_292t1:c.446A>C | NP_009225.1:p.Glu149Ala | |
| NM_007297.3:c.305A>C | NP_009228.2:p.Glu102Ala | |
| NM_007298.3:c.446A>C | NP_009229.2:p.Glu149Ala | |
| NM_007299.3:c.446A>C | NP_009230.2:p.Glu149Ala | |
| NM_007300.3:c.446A>C | NP_009231.2:p.Glu149Ala | |
| NR_027676.1:n.582A>C | ||
| NM_007294.4:c.446A>C MANE Select | NP_009225.1:p.Glu149Ala | |
| NM_007297.4:c.305A>C | NP_009228.2:p.Glu102Ala | |
| NM_007299.4:c.446A>C | NP_009230.2:p.Glu149Ala | |
| NM_007300.4:c.446A>C | NP_009231.2:p.Glu149Ala | |
| NR_027676.2:n.623A>C |