Canonical Allele Identifier: CA3341531

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90783852C>G , CM000667.2:g.90783852C>G	GRCh38
NC_000005.9:g.90079669C>G , CM000667.1:g.90079669C>G	GRCh37
NC_000005.8:g.90115425C>G	NCBI36
NG_007083.1:g.230053C>G
NG_007083.2:g.259509C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13448C>G MANE Select	NP_115495.3:p.Pro4483Arg
ENST00000405460.9:c.13448C>G MANE Select	ENSP00000384582.2:p.Pro4483Arg
NM_032119.3:c.13448C>G	NP_115495.3:p.Pro4483Arg
NR_003149.1:n.13461C>G
NR_003149.2:n.13464C>G
ENST00000405460.6:c.13448C>G	ENSP00000384582.2:p.Pro4483Arg
ENST00000425867.2:c.431C>G	ENSP00000392618.2:p.Pro144Arg
ENST00000425867.3:c.2402C>G	ENSP00000392618.3:p.Pro801Arg
ENST00000638510.1:n.715C>G
ENST00000638975.1:c.77C>G	ENSP00000492630.1:p.Pro26Arg
ENST00000639431.1:c.265+107643C>G	ENSP00000491057.1:n.265+107643C>G
XM_011543675.1:c.13445C>G	XP_011541977.1:p.Pro4482Arg
XM_011543676.1:c.13367C>G	XP_011541978.1:p.Pro4456Arg
XM_011543677.1:c.10751C>G	XP_011541979.1:p.Pro3584Arg
XM_011543678.1:c.13448C>G	XP_011541980.1:p.Pro4483Arg
XM_017009963.2:c.13469C>G	XP_016865452.1:p.Pro4490Arg
XM_017009964.2:c.13466C>G	XP_016865453.1:p.Pro4489Arg
XM_017009965.1:c.13466C>G	XP_016865454.1:p.Pro4489Arg
XM_017009966.2:c.13388C>G	XP_016865455.1:p.Pro4463Arg
XM_017009967.1:c.13373C>G	XP_016865456.1:p.Pro4458Arg
XM_017009968.2:c.13469C>G	XP_016865457.1:p.Pro4490Arg
XM_017009969.2:c.13469C>G	XP_016865458.1:p.Pro4490Arg
XM_017009970.2:c.13469C>G	XP_016865459.1:p.Pro4490Arg
XM_017009971.2:c.13469C>G	XP_016865460.1:p.Pro4490Arg
XM_017009972.1:c.6587C>G	XP_016865461.1:p.Pro2196Arg
XM_017009973.1:c.6566C>G	XP_016865462.1:p.Pro2189Arg