Canonical Allele Identifier: CA1562870617

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716641T= , CM000667.2:g.90716641T=	GRCh38
NC_000005.9:g.90012458T= , CM000667.1:g.90012458T=	GRCh37
NC_000005.8:g.90048214T=	NCBI36
NG_007083.1:g.162842T=
NG_007083.2:g.192298T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9359T= MANE Select	ENSP00000384582.2:p.Ile3120=
ENST00000639431.1:c.265+40432T=	ENSP00000491057.1:n.265+40432T=
ENST00000639473.1:n.4818T=
ENST00000640012.1:c.3166T=
ENST00000640374.1:n.2503T=
ENST00000640779.1:c.4088T=
ENST00000405460.6:c.9359T=	ENSP00000384582.2:p.Ile3120=
ENST00000509621.1:c.2056T=
NM_032119.3:c.9359T=	NP_115495.3:p.Ile3120=
NR_003149.1:n.9372T=
XM_011543675.1:c.9356T=	XP_011541977.1:p.Ile3119=
XM_011543676.1:c.9278T=	XP_011541978.1:p.Ile3093=
XM_011543677.1:c.6662T=	XP_011541979.1:p.Ile2221=
XM_011543678.1:c.9359T=	XP_011541980.1:p.Ile3120=
XM_011543679.1:c.9359T=	XP_011541981.1:p.Ile3120=
XR_948560.1:n.272-832A=
NM_032119.4:c.9359T= MANE Select	NP_115495.3:p.Ile3120=
XM_017009963.2:c.9380T=	XP_016865452.1:p.Ile3127=
XM_017009964.2:c.9377T=	XP_016865453.1:p.Ile3126=
XM_017009965.1:c.9377T=	XP_016865454.1:p.Ile3126=
XM_017009966.2:c.9299T=	XP_016865455.1:p.Ile3100=
XM_017009967.1:c.9284T=	XP_016865456.1:p.Ile3095=
XM_017009968.2:c.9380T=	XP_016865457.1:p.Ile3127=
XM_017009969.2:c.9380T=	XP_016865458.1:p.Ile3127=
XM_017009970.2:c.9380T=	XP_016865459.1:p.Ile3127=
XM_017009971.2:c.9380T=	XP_016865460.1:p.Ile3127=
XM_017009972.1:c.2498T=	XP_016865461.1:p.Ile833=
XM_017009973.1:c.2477T=	XP_016865462.1:p.Ile826=
XM_017009974.2:c.9380T=	XP_016865463.1:p.Ile3127=
XR_001742802.1:n.2523-832A=
NR_003149.2:n.9375T=