Canonical Allele Identifier: CA3341060

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90757048C>G , CM000667.2:g.90757048C>G	GRCh38
NC_000005.9:g.90052865C>G , CM000667.1:g.90052865C>G	GRCh37
NC_000005.8:g.90088621C>G	NCBI36
NG_007083.1:g.203249C>G
NG_007083.2:g.232705C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11827C>G MANE Select	NP_115495.3:p.Arg3943Gly
ENST00000405460.9:c.11827C>G MANE Select	ENSP00000384582.2:p.Arg3943Gly
NM_032119.3:c.11827C>G	NP_115495.3:p.Arg3943Gly
NR_003149.1:n.11840C>G
NR_003149.2:n.11843C>G
ENST00000405460.6:c.11827C>G	ENSP00000384582.2:p.Arg3943Gly
ENST00000425867.3:c.781C>G	ENSP00000392618.3:p.Arg261Gly
ENST00000509621.1:c.4524C>G
ENST00000639431.1:c.265+80839C>G	ENSP00000491057.1:n.265+80839C>G
ENST00000639884.1:n.481C>G
ENST00000640374.1:n.4794C>G
ENST00000640464.1:n.2246C>G
XM_011543675.1:c.11824C>G	XP_011541977.1:p.Arg3942Gly
XM_011543676.1:c.11746C>G	XP_011541978.1:p.Arg3916Gly
XM_011543677.1:c.9130C>G	XP_011541979.1:p.Arg3044Gly
XM_011543678.1:c.11827C>G	XP_011541980.1:p.Arg3943Gly
XM_017009963.2:c.11848C>G	XP_016865452.1:p.Arg3950Gly
XM_017009964.2:c.11845C>G	XP_016865453.1:p.Arg3949Gly
XM_017009965.1:c.11845C>G	XP_016865454.1:p.Arg3949Gly
XM_017009966.2:c.11767C>G	XP_016865455.1:p.Arg3923Gly
XM_017009967.1:c.11752C>G	XP_016865456.1:p.Arg3918Gly
XM_017009968.2:c.11848C>G	XP_016865457.1:p.Arg3950Gly
XM_017009969.2:c.11848C>G	XP_016865458.1:p.Arg3950Gly
XM_017009970.2:c.11848C>G	XP_016865459.1:p.Arg3950Gly
XM_017009971.2:c.11848C>G	XP_016865460.1:p.Arg3950Gly
XM_017009972.1:c.4966C>G	XP_016865461.1:p.Arg1656Gly
XM_017009973.1:c.4945C>G	XP_016865462.1:p.Arg1649Gly