Canonical Allele Identifier: CA3341182

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763441C>G , CM000667.2:g.90763441C>G	GRCh38
NC_000005.9:g.90059258C>G , CM000667.1:g.90059258C>G	GRCh37
NC_000005.8:g.90095014C>G	NCBI36
NG_007083.1:g.209642C>G
NG_007083.2:g.239098C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12257C>G MANE Select	NP_115495.3:p.Pro4086Arg
ENST00000405460.9:c.12257C>G MANE Select	ENSP00000384582.2:p.Pro4086Arg
NM_032119.3:c.12257C>G	NP_115495.3:p.Pro4086Arg
NR_003149.1:n.12270C>G
NR_003149.2:n.12273C>G
ENST00000405460.6:c.12257C>G	ENSP00000384582.2:p.Pro4086Arg
ENST00000425867.3:c.1211C>G	ENSP00000392618.3:p.Pro404Arg
ENST00000639431.1:c.265+87232C>G	ENSP00000491057.1:n.265+87232C>G
ENST00000640464.1:n.2676C>G
ENST00000640729.1:n.834C>G
XM_011543675.1:c.12254C>G	XP_011541977.1:p.Pro4085Arg
XM_011543676.1:c.12176C>G	XP_011541978.1:p.Pro4059Arg
XM_011543677.1:c.9560C>G	XP_011541979.1:p.Pro3187Arg
XM_011543678.1:c.12257C>G	XP_011541980.1:p.Pro4086Arg
XM_017009963.2:c.12278C>G	XP_016865452.1:p.Pro4093Arg
XM_017009964.2:c.12275C>G	XP_016865453.1:p.Pro4092Arg
XM_017009965.1:c.12275C>G	XP_016865454.1:p.Pro4092Arg
XM_017009966.2:c.12197C>G	XP_016865455.1:p.Pro4066Arg
XM_017009967.1:c.12182C>G	XP_016865456.1:p.Pro4061Arg
XM_017009968.2:c.12278C>G	XP_016865457.1:p.Pro4093Arg
XM_017009969.2:c.12278C>G	XP_016865458.1:p.Pro4093Arg
XM_017009970.2:c.12278C>G	XP_016865459.1:p.Pro4093Arg
XM_017009971.2:c.12278C>G	XP_016865460.1:p.Pro4093Arg
XM_017009972.1:c.5396C>G	XP_016865461.1:p.Pro1799Arg
XM_017009973.1:c.5375C>G	XP_016865462.1:p.Pro1792Arg