Canonical Allele Identifier: CA3339939

Gene: ADGRV1

Linked Data

• dbSNP Id: rs770308858
• ExAC: 5:89988429 A / G
• gnomAD v2: 5-89988429-A-G
• gnomAD v4: 5-90692612-A-G
• MyVariant Identifiers: chr5:g.89988429A>G (hg19) ; chr5:g.90692612A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692612A>G , CM000667.2:g.90692612A>G	GRCh38
NC_000005.9:g.89988429A>G , CM000667.1:g.89988429A>G	GRCh37
NC_000005.8:g.90024185A>G	NCBI36
NG_007083.1:g.138813A>G
NG_007083.2:g.168269A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6959A>G MANE Select	ENSP00000384582.2:p.Gln2320Arg
ENST00000639431.1:c.265+16403A>G	ENSP00000491057.1:n.265+16403A>G
ENST00000639473.1:n.2418A>G
ENST00000640012.1:c.766A>G
ENST00000640374.1:n.103A>G
ENST00000640403.1:c.4250A>G	ENSP00000492531.1:p.Gln1417Arg
ENST00000640779.1:c.1688A>G
ENST00000405460.6:c.6959A>G	ENSP00000384582.2:p.Gln2320Arg
NM_032119.3:c.6959A>G	NP_115495.3:p.Gln2320Arg
NR_003149.1:n.6972A>G
XM_011543675.1:c.6956A>G	XP_011541977.1:p.Gln2319Arg
XM_011543676.1:c.6878A>G	XP_011541978.1:p.Gln2293Arg
XM_011543677.1:c.4262A>G	XP_011541979.1:p.Gln1421Arg
XM_011543678.1:c.6959A>G	XP_011541980.1:p.Gln2320Arg
XM_011543679.1:c.6959A>G	XP_011541981.1:p.Gln2320Arg
NM_032119.4:c.6959A>G MANE Select	NP_115495.3:p.Gln2320Arg
XM_017009963.2:c.6959A>G	XP_016865452.1:p.Gln2320Arg
XM_017009964.2:c.6956A>G	XP_016865453.1:p.Gln2319Arg
XM_017009965.1:c.6956A>G	XP_016865454.1:p.Gln2319Arg
XM_017009966.2:c.6878A>G	XP_016865455.1:p.Gln2293Arg
XM_017009967.1:c.6863A>G	XP_016865456.1:p.Gln2288Arg
XM_017009968.2:c.6959A>G	XP_016865457.1:p.Gln2320Arg
XM_017009969.2:c.6959A>G	XP_016865458.1:p.Gln2320Arg
XM_017009970.2:c.6959A>G	XP_016865459.1:p.Gln2320Arg
XM_017009971.2:c.6959A>G	XP_016865460.1:p.Gln2320Arg
XM_017009972.1:c.77A>G	XP_016865461.1:p.Gln26Arg
XM_017009973.1:c.77A>G	XP_016865462.1:p.Gln26Arg
XM_017009974.2:c.6959A>G	XP_016865463.1:p.Gln2320Arg
NR_003149.2:n.6975A>G