Canonical Allele Identifier: CA1562855222

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684207T= , CM000667.2:g.90684207T=	GRCh38
NC_000005.9:g.89980024T= , CM000667.1:g.89980024T=	GRCh37
NC_000005.8:g.90015780T=	NCBI36
NG_007083.1:g.130408T=
NG_007083.2:g.159864T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6274+12T= MANE Select	ENSP00000384582.2:n.6274+12T=
ENST00000639431.1:c.265+7998T=	ENSP00000491057.1:n.265+7998T=
ENST00000639473.1:n.1733+12T=
ENST00000640012.1:c.165-1573T=
ENST00000640403.1:c.3565+12T=	ENSP00000492531.1:n.3565+12T=
ENST00000640779.1:c.1086+12T=
ENST00000405460.6:c.6274+12T=	ENSP00000384582.2:n.6274+12T=
NM_032119.3:c.6274+12T=	NP_115495.3:n.6274+12T=
NR_003149.1:n.6370+12T=
XM_011543675.1:c.6271+12T=	XP_011541977.1:n.6271+12T=
XM_011543676.1:c.6193+12T=	XP_011541978.1:n.6193+12T=
XM_011543677.1:c.3577+12T=	XP_011541979.1:n.3577+12T=
XM_011543678.1:c.6274+12T=	XP_011541980.1:n.6274+12T=
XM_011543679.1:c.6274+12T=	XP_011541981.1:n.6274+12T=
NM_032119.4:c.6274+12T= MANE Select	NP_115495.3:n.6274+12T=
XM_017009963.2:c.6274+12T=	XP_016865452.1:n.6274+12T=
XM_017009964.2:c.6271+12T=	XP_016865453.1:n.6271+12T=
XM_017009965.1:c.6271+12T=	XP_016865454.1:n.6271+12T=
XM_017009966.2:c.6193+12T=	XP_016865455.1:n.6193+12T=
XM_017009967.1:c.6178+12T=	XP_016865456.1:n.6178+12T=
XM_017009968.2:c.6274+12T=	XP_016865457.1:n.6274+12T=
XM_017009969.2:c.6274+12T=	XP_016865458.1:n.6274+12T=
XM_017009970.2:c.6274+12T=	XP_016865459.1:n.6274+12T=
XM_017009971.2:c.6274+12T=	XP_016865460.1:n.6274+12T=
XM_017009973.1:c.-526+12T=	XP_016865462.1:n.-526+12T=
XM_017009974.2:c.6274+12T=	XP_016865463.1:n.6274+12T=
NR_003149.2:n.6373+12T=