Canonical Allele Identifier: CA3339821

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90689896T>A , CM000667.2:g.90689896T>A	GRCh38
NC_000005.9:g.89985713T>A , CM000667.1:g.89985713T>A	GRCh37
NC_000005.8:g.90021469T>A	NCBI36
NG_007083.1:g.136097T>A
NG_007083.2:g.165553T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.6526T>A MANE Select	NP_115495.3:p.Leu2176Met
ENST00000405460.9:c.6526T>A MANE Select	ENSP00000384582.2:p.Leu2176Met
NM_032119.3:c.6526T>A	NP_115495.3:p.Leu2176Met
NR_003149.1:n.6622T>A
NR_003149.2:n.6625T>A
ENST00000405460.6:c.6526T>A	ENSP00000384582.2:p.Leu2176Met
ENST00000639431.1:c.265+13687T>A	ENSP00000491057.1:n.265+13687T>A
ENST00000639473.1:n.1985T>A
ENST00000640012.1:c.416T>A
ENST00000640403.1:c.3817T>A	ENSP00000492531.1:p.Leu1273Met
ENST00000640779.1:c.1338T>A
XM_011543675.1:c.6523T>A	XP_011541977.1:p.Leu2175Met
XM_011543676.1:c.6445T>A	XP_011541978.1:p.Leu2149Met
XM_011543677.1:c.3829T>A	XP_011541979.1:p.Leu1277Met
XM_011543678.1:c.6526T>A	XP_011541980.1:p.Leu2176Met
XM_011543679.1:c.6526T>A	XP_011541981.1:p.Leu2176Met
XM_017009963.2:c.6526T>A	XP_016865452.1:p.Leu2176Met
XM_017009964.2:c.6523T>A	XP_016865453.1:p.Leu2175Met
XM_017009965.1:c.6523T>A	XP_016865454.1:p.Leu2175Met
XM_017009966.2:c.6445T>A	XP_016865455.1:p.Leu2149Met
XM_017009967.1:c.6430T>A	XP_016865456.1:p.Leu2144Met
XM_017009968.2:c.6526T>A	XP_016865457.1:p.Leu2176Met
XM_017009969.2:c.6526T>A	XP_016865458.1:p.Leu2176Met
XM_017009970.2:c.6526T>A	XP_016865459.1:p.Leu2176Met
XM_017009971.2:c.6526T>A	XP_016865460.1:p.Leu2176Met
XM_017009972.1:c.-274T>A	XP_016865461.1:n.-274T>A
XM_017009973.1:c.-274T>A	XP_016865462.1:n.-274T>A
XM_017009974.2:c.6526T>A	XP_016865463.1:p.Leu2176Met