Canonical Allele Identifier: CA445404621

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1746653451
• gnomAD v3: 5-90692781-G-A
• gnomAD v4: 5-90692781-G-A
• MyVariant Identifiers: chr5:g.89988598G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692781G>A , CM000667.2:g.90692781G>A	GRCh38
NC_000005.9:g.89988598G>A , CM000667.1:g.89988598G>A	GRCh37
NC_000005.8:g.90024354G>A	NCBI36
NG_007083.1:g.138982G>A
NG_007083.2:g.168438G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7128G>A MANE Select	ENSP00000384582.2:p.Arg2376=
ENST00000639431.1:c.265+16572G>A	ENSP00000491057.1:n.265+16572G>A
ENST00000639473.1:n.2587G>A
ENST00000640012.1:c.935G>A
ENST00000640374.1:n.272G>A
ENST00000640403.1:c.4419G>A	ENSP00000492531.1:p.Arg1473=
ENST00000640779.1:c.1857G>A
ENST00000405460.6:c.7128G>A	ENSP00000384582.2:p.Arg2376=
NM_032119.3:c.7128G>A	NP_115495.3:p.Arg2376=
NR_003149.1:n.7141G>A
XM_011543675.1:c.7125G>A	XP_011541977.1:p.Arg2375=
XM_011543676.1:c.7047G>A	XP_011541978.1:p.Arg2349=
XM_011543677.1:c.4431G>A	XP_011541979.1:p.Arg1477=
XM_011543678.1:c.7128G>A	XP_011541980.1:p.Arg2376=
XM_011543679.1:c.7128G>A	XP_011541981.1:p.Arg2376=
NM_032119.4:c.7128G>A MANE Select	NP_115495.3:p.Arg2376=
XM_017009963.2:c.7128G>A	XP_016865452.1:p.Arg2376=
XM_017009964.2:c.7125G>A	XP_016865453.1:p.Arg2375=
XM_017009965.1:c.7125G>A	XP_016865454.1:p.Arg2375=
XM_017009966.2:c.7047G>A	XP_016865455.1:p.Arg2349=
XM_017009967.1:c.7032G>A	XP_016865456.1:p.Arg2344=
XM_017009968.2:c.7128G>A	XP_016865457.1:p.Arg2376=
XM_017009969.2:c.7128G>A	XP_016865458.1:p.Arg2376=
XM_017009970.2:c.7128G>A	XP_016865459.1:p.Arg2376=
XM_017009971.2:c.7128G>A	XP_016865460.1:p.Arg2376=
XM_017009972.1:c.246G>A	XP_016865461.1:p.Arg82=
XM_017009973.1:c.246G>A	XP_016865462.1:p.Arg82=
XM_017009974.2:c.7128G>A	XP_016865463.1:p.Arg2376=
NR_003149.2:n.7144G>A