Canonical Allele Identifier: CA360371810

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1209258737
• gnomAD v4: 5-90692752-A-G
• MyVariant Identifiers: chr5:g.89988569A>G (hg19) ; chr5:g.90692752A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692752A>G , CM000667.2:g.90692752A>G	GRCh38
NC_000005.9:g.89988569A>G , CM000667.1:g.89988569A>G	GRCh37
NC_000005.8:g.90024325A>G	NCBI36
NG_007083.1:g.138953A>G
NG_007083.2:g.168409A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7099A>G MANE Select	ENSP00000384582.2:p.Arg2367Gly
ENST00000639431.1:c.265+16543A>G	ENSP00000491057.1:n.265+16543A>G
ENST00000639473.1:n.2558A>G
ENST00000640012.1:c.906A>G
ENST00000640374.1:n.243A>G
ENST00000640403.1:c.4390A>G	ENSP00000492531.1:p.Arg1464Gly
ENST00000640779.1:c.1828A>G
ENST00000405460.6:c.7099A>G	ENSP00000384582.2:p.Arg2367Gly
NM_032119.3:c.7099A>G	NP_115495.3:p.Arg2367Gly
NR_003149.1:n.7112A>G
XM_011543675.1:c.7096A>G	XP_011541977.1:p.Arg2366Gly
XM_011543676.1:c.7018A>G	XP_011541978.1:p.Arg2340Gly
XM_011543677.1:c.4402A>G	XP_011541979.1:p.Arg1468Gly
XM_011543678.1:c.7099A>G	XP_011541980.1:p.Arg2367Gly
XM_011543679.1:c.7099A>G	XP_011541981.1:p.Arg2367Gly
NM_032119.4:c.7099A>G MANE Select	NP_115495.3:p.Arg2367Gly
XM_017009963.2:c.7099A>G	XP_016865452.1:p.Arg2367Gly
XM_017009964.2:c.7096A>G	XP_016865453.1:p.Arg2366Gly
XM_017009965.1:c.7096A>G	XP_016865454.1:p.Arg2366Gly
XM_017009966.2:c.7018A>G	XP_016865455.1:p.Arg2340Gly
XM_017009967.1:c.7003A>G	XP_016865456.1:p.Arg2335Gly
XM_017009968.2:c.7099A>G	XP_016865457.1:p.Arg2367Gly
XM_017009969.2:c.7099A>G	XP_016865458.1:p.Arg2367Gly
XM_017009970.2:c.7099A>G	XP_016865459.1:p.Arg2367Gly
XM_017009971.2:c.7099A>G	XP_016865460.1:p.Arg2367Gly
XM_017009972.1:c.217A>G	XP_016865461.1:p.Arg73Gly
XM_017009973.1:c.217A>G	XP_016865462.1:p.Arg73Gly
XM_017009974.2:c.7099A>G	XP_016865463.1:p.Arg2367Gly
NR_003149.2:n.7115A>G