Linked Data
ClinVar Variation Id:
2112541
ClinVar RCV Id:
RCV003026877
dbSNP Id:
rs1014876003
gnomAD v4:
8-93758499-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.93758499A>T , CM000670.2:g.93758499A>T | GRCh38 |
| NC_000008.10:g.94770727A>T , CM000670.1:g.94770727A>T | GRCh37 |
| NC_000008.9:g.94839903A>T | NCBI36 |
| NG_009190.1:g.8656A>T , LRG_688:g.8656A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323130.8:c.329A>T | ENSP00000314488.4:p.Asp110Val | |
| ENST00000409623.8:c.329A>T | ENSP00000386966.4:p.Asp110Val | |
| ENST00000452276.6:c.329A>T | ENSP00000388671.2:p.Asp110Val | |
| ENST00000453906.6:c.329A>T | ENSP00000403035.2:p.Asp110Val | |
| ENST00000520680.2:c.329A>T | ENSP00000428785.2:p.Asp110Val | |
| ENST00000521065.2:c.329A>T | ENSP00000427947.2:p.Asp110Val | |
| ENST00000521517.6:c.329A>T | ENSP00000430740.2:p.Asp110Val | |
| ENST00000681998.1:c.329A>T | ENSP00000506773.1:p.Asp110Val | |
| ENST00000682036.1:c.329A>T | ENSP00000508390.1:p.Asp110Val | |
| ENST00000682577.1:c.329A>T | ENSP00000506963.1:p.Asp110Val | |
| ENST00000682624.1:c.240A>T | ENSP00000508343.1:p.Arg80Ser | |
| ENST00000682700.1:c.329A>T | ENSP00000507627.1:p.Asp110Val | |
| ENST00000682804.1:n.222A>T | ||
| ENST00000682837.1:c.329A>T | ENSP00000507920.1:p.Asp110Val | |
| ENST00000682935.1:n.329A>T | ||
| ENST00000682984.1:c.312+2633A>T | ENSP00000507209.1:n.312+2633A>T | |
| ENST00000683078.1:c.329A>T | ENSP00000506796.1:p.Asp110Val | |
| ENST00000683223.1:c.240A>T | ENSP00000507685.1:p.Arg80Ser | |
| ENST00000683238.1:n.150A>T | ||
| ENST00000683249.1:n.350A>T | ||
| ENST00000683336.1:c.329A>T | ENSP00000507695.1:p.Asp110Val | |
| ENST00000683362.1:c.312+2633A>T | ENSP00000506985.1:n.312+2633A>T | |
| ENST00000683850.1:n.252A>T | ||
| ENST00000683919.1:c.329A>T | ENSP00000507617.1:p.Asp110Val | |
| ENST00000683953.1:c.240A>T | ENSP00000508375.1:p.Arg80Ser | |
| ENST00000684023.1:c.329A>T | ENSP00000507461.1:p.Asp110Val | |
| ENST00000684064.1:c.20A>T | ENSP00000508192.1:p.Asp7Val | |
| ENST00000684089.1:n.319A>T | ||
| ENST00000684149.1:c.329A>T | ENSP00000507943.1:p.Asp110Val | |
| ENST00000684416.1:n.154A>T | ||
| ENST00000684540.1:c.329A>T | ENSP00000507987.1:p.Asp110Val | |
| ENST00000684733.1:n.264A>T | ||
| ENST00000453321.8:c.329A>T MANE Select | ENSP00000389998.3:p.Asp110Val | |
| ENST00000323130.7:c.299A>T | ENSP00000314488.3:p.Asp100Val | |
| ENST00000409623.7:c.-49A>T | ENSP00000386966.3:n.-49A>T | |
| ENST00000452276.5:c.20A>T | ENSP00000388671.1:p.Asp7Val | |
| ENST00000453321.7:c.329A>T | ENSP00000389998.3:p.Asp110Val | |
| ENST00000453906.5:c.329A>T | ENSP00000403035.1:p.Asp110Val | |
| ENST00000455946.5:c.329A>T | ENSP00000416339.1:p.Asp110Val | |
| ENST00000474944.5:n.349A>T | ||
| ENST00000475305.1:n.338A>T | ||
| ENST00000498673.5:c.-152A>T | ENSP00000430232.1:n.-152A>T | |
| ENST00000518319.5:c.-191A>T | ENSP00000430289.1:n.-191A>T | |
| ENST00000521065.1:c.235A>T | ||
| ENST00000521222.5:c.325A>T | ENSP00000429925.1:p.Met109Leu | |
| ENST00000521517.5:c.321A>T | ||
| NM_001142301.1:c.-49A>T , LRG_688t2:c.-49A>T | NP_001135773.1:n.-49A>T | |
| NM_153704.5:c.329A>T , LRG_688t1:c.329A>T | NP_714915.3:p.Asp110Val | |
| NR_024522.1:n.400A>T | ||
| XM_006716686.2:c.26A>T | XP_006716749.1:p.Asp9Val | |
| XM_011517363.1:c.329A>T | XP_011515665.1:p.Asp110Val | |
| XR_428387.1:n.387A>T | ||
| XR_928360.1:n.387A>T | ||
| XR_928361.1:n.387A>T | ||
| XR_928362.1:n.387A>T | ||
| XM_006716686.4:c.26A>T | XP_006716749.1:p.Asp9Val | |
| XM_011517363.3:c.329A>T | XP_011515665.1:p.Asp110Val | |
| XM_024447326.1:c.-81A>T | XP_024303094.1:n.-81A>T | |
| XR_001745619.2:n.370A>T | ||
| XR_428387.2:n.370A>T | ||
| XR_928360.3:n.370A>T | ||
| XR_928362.3:n.370A>T | ||
| NM_153704.6:c.329A>T MANE Select | NP_714915.3:p.Asp110Val | |
| NR_024522.2:n.350A>T |