Canonical Allele Identifier: CA122798454

Gene: ADGRV1

Linked Data

• dbSNP Id: rs371966463
• MyVariant Identifiers: chr5:g.90050866A>G (hg19) ; chr5:g.90755049A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755049A>G , CM000667.2:g.90755049A>G	GRCh38
NC_000005.9:g.90050866A>G , CM000667.1:g.90050866A>G	GRCh37
NC_000005.8:g.90086622A>G	NCBI36
NG_007083.1:g.201250A>G
NG_007083.2:g.230706A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11444A>G MANE Select	ENSP00000384582.2:p.His3815Arg
ENST00000425867.3:c.575A>G	ENSP00000392618.3:p.His192Arg
ENST00000639431.1:c.265+78840A>G	ENSP00000491057.1:n.265+78840A>G
ENST00000640374.1:n.4588A>G
ENST00000640464.1:n.1863A>G
ENST00000405460.6:c.11444A>G	ENSP00000384582.2:p.His3815Arg
ENST00000509621.1:c.4141A>G
NM_032119.3:c.11444A>G	NP_115495.3:p.His3815Arg
NR_003149.1:n.11457A>G
XM_011543675.1:c.11441A>G	XP_011541977.1:p.His3814Arg
XM_011543676.1:c.11363A>G	XP_011541978.1:p.His3788Arg
XM_011543677.1:c.8747A>G	XP_011541979.1:p.His2916Arg
XM_011543678.1:c.11444A>G	XP_011541980.1:p.His3815Arg
NM_032119.4:c.11444A>G MANE Select	NP_115495.3:p.His3815Arg
XM_017009963.2:c.11465A>G	XP_016865452.1:p.His3822Arg
XM_017009964.2:c.11462A>G	XP_016865453.1:p.His3821Arg
XM_017009965.1:c.11462A>G	XP_016865454.1:p.His3821Arg
XM_017009966.2:c.11384A>G	XP_016865455.1:p.His3795Arg
XM_017009967.1:c.11369A>G	XP_016865456.1:p.His3790Arg
XM_017009968.2:c.11465A>G	XP_016865457.1:p.His3822Arg
XM_017009969.2:c.11465A>G	XP_016865458.1:p.His3822Arg
XM_017009970.2:c.11465A>G	XP_016865459.1:p.His3822Arg
XM_017009971.2:c.11465A>G	XP_016865460.1:p.His3822Arg
XM_017009972.1:c.4583A>G	XP_016865461.1:p.His1528Arg
XM_017009973.1:c.4562A>G	XP_016865462.1:p.His1521Arg
NR_003149.2:n.11460A>G