Canonical Allele Identifier: CA360396127

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712294-A-G
• MyVariant Identifiers: chr5:g.90008111A>G (hg19) ; chr5:g.90712294A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712294A>G , CM000667.2:g.90712294A>G	GRCh38
NC_000005.9:g.90008111A>G , CM000667.1:g.90008111A>G	GRCh37
NC_000005.8:g.90043867A>G	NCBI36
NG_007083.1:g.158495A>G
NG_007083.2:g.187951A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9050A>G MANE Select	ENSP00000384582.2:p.His3017Arg
ENST00000639431.1:c.265+36085A>G	ENSP00000491057.1:n.265+36085A>G
ENST00000639473.1:n.4509A>G
ENST00000640012.1:c.2857A>G
ENST00000640374.1:n.2194A>G
ENST00000640779.1:c.3779A>G
ENST00000405460.6:c.9050A>G	ENSP00000384582.2:p.His3017Arg
ENST00000509621.1:c.1747A>G
NM_032119.3:c.9050A>G	NP_115495.3:p.His3017Arg
NR_003149.1:n.9063A>G
XM_011543675.1:c.9047A>G	XP_011541977.1:p.His3016Arg
XM_011543676.1:c.8969A>G	XP_011541978.1:p.His2990Arg
XM_011543677.1:c.6353A>G	XP_011541979.1:p.His2118Arg
XM_011543678.1:c.9050A>G	XP_011541980.1:p.His3017Arg
XM_011543679.1:c.9050A>G	XP_011541981.1:p.His3017Arg
NM_032119.4:c.9050A>G MANE Select	NP_115495.3:p.His3017Arg
XM_017009963.2:c.9071A>G	XP_016865452.1:p.His3024Arg
XM_017009964.2:c.9068A>G	XP_016865453.1:p.His3023Arg
XM_017009965.1:c.9068A>G	XP_016865454.1:p.His3023Arg
XM_017009966.2:c.8990A>G	XP_016865455.1:p.His2997Arg
XM_017009967.1:c.8975A>G	XP_016865456.1:p.His2992Arg
XM_017009968.2:c.9071A>G	XP_016865457.1:p.His3024Arg
XM_017009969.2:c.9071A>G	XP_016865458.1:p.His3024Arg
XM_017009970.2:c.9071A>G	XP_016865459.1:p.His3024Arg
XM_017009971.2:c.9071A>G	XP_016865460.1:p.His3024Arg
XM_017009972.1:c.2189A>G	XP_016865461.1:p.His730Arg
XM_017009973.1:c.2168A>G	XP_016865462.1:p.His723Arg
XM_017009974.2:c.9071A>G	XP_016865463.1:p.His3024Arg
NR_003149.2:n.9066A>G