Canonical Allele Identifier: CA360366752

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90755079-A-G
• MyVariant Identifiers: chr5:g.90050896A>G (hg19) ; chr5:g.90755079A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755079A>G , CM000667.2:g.90755079A>G	GRCh38
NC_000005.9:g.90050896A>G , CM000667.1:g.90050896A>G	GRCh37
NC_000005.8:g.90086652A>G	NCBI36
NG_007083.1:g.201280A>G
NG_007083.2:g.230736A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11474A>G MANE Select	ENSP00000384582.2:p.His3825Arg
ENST00000425867.3:c.605A>G	ENSP00000392618.3:p.His202Arg
ENST00000639431.1:c.265+78870A>G	ENSP00000491057.1:n.265+78870A>G
ENST00000640374.1:n.4618A>G
ENST00000640464.1:n.1893A>G
ENST00000405460.6:c.11474A>G	ENSP00000384582.2:p.His3825Arg
ENST00000509621.1:c.4171A>G
NM_032119.3:c.11474A>G	NP_115495.3:p.His3825Arg
NR_003149.1:n.11487A>G
XM_011543675.1:c.11471A>G	XP_011541977.1:p.His3824Arg
XM_011543676.1:c.11393A>G	XP_011541978.1:p.His3798Arg
XM_011543677.1:c.8777A>G	XP_011541979.1:p.His2926Arg
XM_011543678.1:c.11474A>G	XP_011541980.1:p.His3825Arg
NM_032119.4:c.11474A>G MANE Select	NP_115495.3:p.His3825Arg
XM_017009963.2:c.11495A>G	XP_016865452.1:p.His3832Arg
XM_017009964.2:c.11492A>G	XP_016865453.1:p.His3831Arg
XM_017009965.1:c.11492A>G	XP_016865454.1:p.His3831Arg
XM_017009966.2:c.11414A>G	XP_016865455.1:p.His3805Arg
XM_017009967.1:c.11399A>G	XP_016865456.1:p.His3800Arg
XM_017009968.2:c.11495A>G	XP_016865457.1:p.His3832Arg
XM_017009969.2:c.11495A>G	XP_016865458.1:p.His3832Arg
XM_017009970.2:c.11495A>G	XP_016865459.1:p.His3832Arg
XM_017009971.2:c.11495A>G	XP_016865460.1:p.His3832Arg
XM_017009972.1:c.4613A>G	XP_016865461.1:p.His1538Arg
XM_017009973.1:c.4592A>G	XP_016865462.1:p.His1531Arg
NR_003149.2:n.11490A>G