Canonical Allele Identifier: CA1562864640

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90705508C= , CM000667.2:g.90705508C=	GRCh38
NC_000005.9:g.90001325C= , CM000667.1:g.90001325C=	GRCh37
NC_000005.8:g.90037081C=	NCBI36
NG_007083.1:g.151709C=
NG_007083.2:g.181165C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.8495C= MANE Select	ENSP00000384582.2:p.Ser2832=
ENST00000639431.1:c.265+29299C=	ENSP00000491057.1:n.265+29299C=
ENST00000639473.1:n.3954C=
ENST00000640012.1:c.2302C=
ENST00000640374.1:n.1639C=
ENST00000640403.1:c.5786C=	ENSP00000492531.1:p.Ser1929=
ENST00000640779.1:c.3224C=
ENST00000405460.6:c.8495C=	ENSP00000384582.2:p.Ser2832=
ENST00000509621.1:c.1192C=
NM_032119.3:c.8495C=	NP_115495.3:p.Ser2832=
NR_003149.1:n.8508C=
XM_011543675.1:c.8492C=	XP_011541977.1:p.Ser2831=
XM_011543676.1:c.8414C=	XP_011541978.1:p.Ser2805=
XM_011543677.1:c.5798C=	XP_011541979.1:p.Ser1933=
XM_011543678.1:c.8495C=	XP_011541980.1:p.Ser2832=
XM_011543679.1:c.8495C=	XP_011541981.1:p.Ser2832=
NM_032119.4:c.8495C= MANE Select	NP_115495.3:p.Ser2832=
XM_017009963.2:c.8516C=	XP_016865452.1:p.Ser2839=
XM_017009964.2:c.8513C=	XP_016865453.1:p.Ser2838=
XM_017009965.1:c.8513C=	XP_016865454.1:p.Ser2838=
XM_017009966.2:c.8435C=	XP_016865455.1:p.Ser2812=
XM_017009967.1:c.8420C=	XP_016865456.1:p.Ser2807=
XM_017009968.2:c.8516C=	XP_016865457.1:p.Ser2839=
XM_017009969.2:c.8516C=	XP_016865458.1:p.Ser2839=
XM_017009970.2:c.8516C=	XP_016865459.1:p.Ser2839=
XM_017009971.2:c.8516C=	XP_016865460.1:p.Ser2839=
XM_017009972.1:c.1634C=	XP_016865461.1:p.Ser545=
XM_017009973.1:c.1613C=	XP_016865462.1:p.Ser538=
XM_017009974.2:c.8516C=	XP_016865463.1:p.Ser2839=
NR_003149.2:n.8511C=