Canonical Allele Identifier: CA445404579

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988571A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692754A>G , CM000667.2:g.90692754A>G	GRCh38
NC_000005.9:g.89988571A>G , CM000667.1:g.89988571A>G	GRCh37
NC_000005.8:g.90024327A>G	NCBI36
NG_007083.1:g.138955A>G
NG_007083.2:g.168411A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7101A>G MANE Select	ENSP00000384582.2:p.Arg2367=
ENST00000639431.1:c.265+16545A>G	ENSP00000491057.1:n.265+16545A>G
ENST00000639473.1:n.2560A>G
ENST00000640012.1:c.908A>G
ENST00000640374.1:n.245A>G
ENST00000640403.1:c.4392A>G	ENSP00000492531.1:p.Arg1464=
ENST00000640779.1:c.1830A>G
ENST00000405460.6:c.7101A>G	ENSP00000384582.2:p.Arg2367=
NM_032119.3:c.7101A>G	NP_115495.3:p.Arg2367=
NR_003149.1:n.7114A>G
XM_011543675.1:c.7098A>G	XP_011541977.1:p.Arg2366=
XM_011543676.1:c.7020A>G	XP_011541978.1:p.Arg2340=
XM_011543677.1:c.4404A>G	XP_011541979.1:p.Arg1468=
XM_011543678.1:c.7101A>G	XP_011541980.1:p.Arg2367=
XM_011543679.1:c.7101A>G	XP_011541981.1:p.Arg2367=
NM_032119.4:c.7101A>G MANE Select	NP_115495.3:p.Arg2367=
XM_017009963.2:c.7101A>G	XP_016865452.1:p.Arg2367=
XM_017009964.2:c.7098A>G	XP_016865453.1:p.Arg2366=
XM_017009965.1:c.7098A>G	XP_016865454.1:p.Arg2366=
XM_017009966.2:c.7020A>G	XP_016865455.1:p.Arg2340=
XM_017009967.1:c.7005A>G	XP_016865456.1:p.Arg2335=
XM_017009968.2:c.7101A>G	XP_016865457.1:p.Arg2367=
XM_017009969.2:c.7101A>G	XP_016865458.1:p.Arg2367=
XM_017009970.2:c.7101A>G	XP_016865459.1:p.Arg2367=
XM_017009971.2:c.7101A>G	XP_016865460.1:p.Arg2367=
XM_017009972.1:c.219A>G	XP_016865461.1:p.Arg73=
XM_017009973.1:c.219A>G	XP_016865462.1:p.Arg73=
XM_017009974.2:c.7101A>G	XP_016865463.1:p.Arg2367=
NR_003149.2:n.7117A>G