Canonical Allele Identifier: CA3340983
Gene: ADGRV1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1316081
ClinVar RCV Id: RCV001757528
dbSNP Id: rs780647523
gnomAD v3: 5-90755124-A-T
gnomAD v4: 5-90755124-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755124A>T , CM000667.2:g.90755124A>T GRCh38
NC_000005.9:g.90050941A>T , CM000667.1:g.90050941A>T GRCh37
NC_000005.8:g.90086697A>T NCBI36
NG_007083.1:g.201325A>T
NG_007083.2:g.230781A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11519A>T MANE Select ENSP00000384582.2:p.Glu3840Val
ENST00000425867.3:c.650A>T ENSP00000392618.3:p.Glu217Val
ENST00000639431.1:c.265+78915A>T ENSP00000491057.1:n.265+78915A>T
ENST00000640374.1:n.4663A>T
ENST00000640464.1:n.1938A>T
ENST00000405460.6:c.11519A>T ENSP00000384582.2:p.Glu3840Val
ENST00000509621.1:c.4216A>T
NM_032119.3:c.11519A>T NP_115495.3:p.Glu3840Val
NR_003149.1:n.11532A>T
XM_011543675.1:c.11516A>T XP_011541977.1:p.Glu3839Val
XM_011543676.1:c.11438A>T XP_011541978.1:p.Glu3813Val
XM_011543677.1:c.8822A>T XP_011541979.1:p.Glu2941Val
XM_011543678.1:c.11519A>T XP_011541980.1:p.Glu3840Val
NM_032119.4:c.11519A>T MANE Select NP_115495.3:p.Glu3840Val
XM_017009963.2:c.11540A>T XP_016865452.1:p.Glu3847Val
XM_017009964.2:c.11537A>T XP_016865453.1:p.Glu3846Val
XM_017009965.1:c.11537A>T XP_016865454.1:p.Glu3846Val
XM_017009966.2:c.11459A>T XP_016865455.1:p.Glu3820Val
XM_017009967.1:c.11444A>T XP_016865456.1:p.Glu3815Val
XM_017009968.2:c.11540A>T XP_016865457.1:p.Glu3847Val
XM_017009969.2:c.11540A>T XP_016865458.1:p.Glu3847Val
XM_017009970.2:c.11540A>T XP_016865459.1:p.Glu3847Val
XM_017009971.2:c.11540A>T XP_016865460.1:p.Glu3847Val
XM_017009972.1:c.4658A>T XP_016865461.1:p.Glu1553Val
XM_017009973.1:c.4637A>T XP_016865462.1:p.Glu1546Val
NR_003149.2:n.11535A>T