Canonical Allele Identifier: CA3341707

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791149C>T , CM000667.2:g.90791149C>T	GRCh38
NC_000005.9:g.90086966C>T , CM000667.1:g.90086966C>T	GRCh37
NC_000005.8:g.90122722C>T	NCBI36
NG_007083.1:g.237350C>T
NG_007083.2:g.266806C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14320C>T MANE Select	NP_115495.3:p.Leu4774Phe
ENST00000405460.9:c.14320C>T MANE Select	ENSP00000384582.2:p.Leu4774Phe
NM_032119.3:c.14320C>T	NP_115495.3:p.Leu4774Phe
NR_003149.1:n.14333C>T
NR_003149.2:n.14336C>T
ENST00000405460.6:c.14320C>T	ENSP00000384582.2:p.Leu4774Phe
ENST00000425867.2:c.1303C>T	ENSP00000392618.2:p.Leu435Phe
ENST00000425867.3:c.3274C>T	ENSP00000392618.3:p.Leu1092Phe
ENST00000638510.1:n.1587C>T
ENST00000638585.1:n.86C>T
ENST00000638975.1:c.949C>T	ENSP00000492630.1:p.Leu317Phe
ENST00000639431.1:c.265+114940C>T	ENSP00000491057.1:n.265+114940C>T
ENST00000640407.1:c.730C>T	ENSP00000491425.1:p.Leu244Phe
XM_011543675.1:c.14317C>T	XP_011541977.1:p.Leu4773Phe
XM_011543676.1:c.14239C>T	XP_011541978.1:p.Leu4747Phe
XM_011543677.1:c.11623C>T	XP_011541979.1:p.Leu3875Phe
XM_011543678.1:c.14320C>T	XP_011541980.1:p.Leu4774Phe
XM_017009963.2:c.14341C>T	XP_016865452.1:p.Leu4781Phe
XM_017009964.2:c.14338C>T	XP_016865453.1:p.Leu4780Phe
XM_017009965.1:c.14338C>T	XP_016865454.1:p.Leu4780Phe
XM_017009966.2:c.14260C>T	XP_016865455.1:p.Leu4754Phe
XM_017009967.1:c.14245C>T	XP_016865456.1:p.Leu4749Phe
XM_017009968.2:c.14341C>T	XP_016865457.1:p.Leu4781Phe
XM_017009969.2:c.14341C>T	XP_016865458.1:p.Leu4781Phe
XM_017009970.2:c.14341C>T	XP_016865459.1:p.Leu4781Phe
XM_017009971.2:c.14341C>T	XP_016865460.1:p.Leu4781Phe
XM_017009972.1:c.7459C>T	XP_016865461.1:p.Leu2487Phe
XM_017009973.1:c.7438C>T	XP_016865462.1:p.Leu2480Phe