Canonical Allele Identifier: CA3341227

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90774273A>G , CM000667.2:g.90774273A>G	GRCh38
NC_000005.9:g.90070090A>G , CM000667.1:g.90070090A>G	GRCh37
NC_000005.8:g.90105846A>G	NCBI36
NG_007083.1:g.220474A>G
NG_007083.2:g.249930A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12373A>G MANE Select	NP_115495.3:p.Ile4125Val
ENST00000405460.9:c.12373A>G MANE Select	ENSP00000384582.2:p.Ile4125Val
NM_032119.3:c.12373A>G	NP_115495.3:p.Ile4125Val
NR_003149.1:n.12386A>G
NR_003149.2:n.12389A>G
ENST00000405460.6:c.12373A>G	ENSP00000384582.2:p.Ile4125Val
ENST00000425867.3:c.1327A>G	ENSP00000392618.3:p.Ile443Val
ENST00000639431.1:c.265+98064A>G	ENSP00000491057.1:n.265+98064A>G
ENST00000640464.1:n.2792A>G
ENST00000640729.1:n.950A>G
XM_011543675.1:c.12370A>G	XP_011541977.1:p.Ile4124Val
XM_011543676.1:c.12292A>G	XP_011541978.1:p.Ile4098Val
XM_011543677.1:c.9676A>G	XP_011541979.1:p.Ile3226Val
XM_011543678.1:c.12373A>G	XP_011541980.1:p.Ile4125Val
XM_017009963.2:c.12394A>G	XP_016865452.1:p.Ile4132Val
XM_017009964.2:c.12391A>G	XP_016865453.1:p.Ile4131Val
XM_017009965.1:c.12391A>G	XP_016865454.1:p.Ile4131Val
XM_017009966.2:c.12313A>G	XP_016865455.1:p.Ile4105Val
XM_017009967.1:c.12298A>G	XP_016865456.1:p.Ile4100Val
XM_017009968.2:c.12394A>G	XP_016865457.1:p.Ile4132Val
XM_017009969.2:c.12394A>G	XP_016865458.1:p.Ile4132Val
XM_017009970.2:c.12394A>G	XP_016865459.1:p.Ile4132Val
XM_017009971.2:c.12394A>G	XP_016865460.1:p.Ile4132Val
XM_017009972.1:c.5512A>G	XP_016865461.1:p.Ile1838Val
XM_017009973.1:c.5491A>G	XP_016865462.1:p.Ile1831Val