Canonical Allele Identifier: CA176199
Gene: ADGRV1 HGNC NCBI

Linked Data

ClinVar Variation Id: 163583
dbSNP Id: rs146526977
gnomAD v2: 5-89990440-G-A
gnomAD v3: 5-90694623-G-A
gnomAD v4: 5-90694623-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90694623G>A , CM000667.2:g.90694623G>A GRCh38
NC_000005.9:g.89990440G>A , CM000667.1:g.89990440G>A GRCh37
NC_000005.8:g.90026196G>A NCBI36
NG_007083.1:g.140824G>A
NG_007083.2:g.170280G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7867G>A MANE Select ENSP00000384582.2:p.Glu2623Lys
ENST00000639431.1:c.265+18414G>A ENSP00000491057.1:n.265+18414G>A
ENST00000639473.1:n.3326G>A
ENST00000640012.1:c.1674G>A
ENST00000640374.1:n.1011G>A
ENST00000640403.1:c.5158G>A ENSP00000492531.1:p.Glu1720Lys
ENST00000640779.1:c.2596G>A
ENST00000405460.6:c.7867G>A ENSP00000384582.2:p.Glu2623Lys
ENST00000509621.1:c.564G>A
NM_032119.3:c.7867G>A NP_115495.3:p.Glu2623Lys
NR_003149.1:n.7880G>A
XM_011543675.1:c.7864G>A XP_011541977.1:p.Glu2622Lys
XM_011543676.1:c.7786G>A XP_011541978.1:p.Glu2596Lys
XM_011543677.1:c.5170G>A XP_011541979.1:p.Glu1724Lys
XM_011543678.1:c.7867G>A XP_011541980.1:p.Glu2623Lys
XM_011543679.1:c.7867G>A XP_011541981.1:p.Glu2623Lys
NM_032119.4:c.7867G>A MANE Select NP_115495.3:p.Glu2623Lys
XM_017009963.2:c.7867G>A XP_016865452.1:p.Glu2623Lys
XM_017009964.2:c.7864G>A XP_016865453.1:p.Glu2622Lys
XM_017009965.1:c.7864G>A XP_016865454.1:p.Glu2622Lys
XM_017009966.2:c.7786G>A XP_016865455.1:p.Glu2596Lys
XM_017009967.1:c.7771G>A XP_016865456.1:p.Glu2591Lys
XM_017009968.2:c.7867G>A XP_016865457.1:p.Glu2623Lys
XM_017009969.2:c.7867G>A XP_016865458.1:p.Glu2623Lys
XM_017009970.2:c.7867G>A XP_016865459.1:p.Glu2623Lys
XM_017009971.2:c.7867G>A XP_016865460.1:p.Glu2623Lys
XM_017009972.1:c.985G>A XP_016865461.1:p.Glu329Lys
XM_017009973.1:c.985G>A XP_016865462.1:p.Glu329Lys
XM_017009974.2:c.7867G>A XP_016865463.1:p.Glu2623Lys
NR_003149.2:n.7883G>A