Canonical Allele Identifier: CA1562870626

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716673A= , CM000667.2:g.90716673A=	GRCh38
NC_000005.9:g.90012490A= , CM000667.1:g.90012490A=	GRCh37
NC_000005.8:g.90048246A=	NCBI36
NG_007083.1:g.162874A=
NG_007083.2:g.192330A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9391A= MANE Select	ENSP00000384582.2:p.Lys3131=
ENST00000639431.1:c.265+40464A=	ENSP00000491057.1:n.265+40464A=
ENST00000639473.1:n.4850A=
ENST00000640012.1:c.3198A=
ENST00000640374.1:n.2535A=
ENST00000640779.1:c.4120A=
ENST00000405460.6:c.9391A=	ENSP00000384582.2:p.Lys3131=
ENST00000509621.1:c.2088A=
NM_032119.3:c.9391A=	NP_115495.3:p.Lys3131=
NR_003149.1:n.9404A=
XM_011543675.1:c.9388A=	XP_011541977.1:p.Lys3130=
XM_011543676.1:c.9310A=	XP_011541978.1:p.Lys3104=
XM_011543677.1:c.6694A=	XP_011541979.1:p.Lys2232=
XM_011543678.1:c.9391A=	XP_011541980.1:p.Lys3131=
XM_011543679.1:c.9391A=	XP_011541981.1:p.Lys3131=
XR_948560.1:n.272-864T=
NM_032119.4:c.9391A= MANE Select	NP_115495.3:p.Lys3131=
XM_017009963.2:c.9412A=	XP_016865452.1:p.Lys3138=
XM_017009964.2:c.9409A=	XP_016865453.1:p.Lys3137=
XM_017009965.1:c.9409A=	XP_016865454.1:p.Lys3137=
XM_017009966.2:c.9331A=	XP_016865455.1:p.Lys3111=
XM_017009967.1:c.9316A=	XP_016865456.1:p.Lys3106=
XM_017009968.2:c.9412A=	XP_016865457.1:p.Lys3138=
XM_017009969.2:c.9412A=	XP_016865458.1:p.Lys3138=
XM_017009970.2:c.9412A=	XP_016865459.1:p.Lys3138=
XM_017009971.2:c.9412A=	XP_016865460.1:p.Lys3138=
XM_017009972.1:c.2530A=	XP_016865461.1:p.Lys844=
XM_017009973.1:c.2509A=	XP_016865462.1:p.Lys837=
XM_017009974.2:c.9412A=	XP_016865463.1:p.Lys3138=
XR_001742802.1:n.2523-864T=
NR_003149.2:n.9407A=