Canonical Allele Identifier: CA1562874885

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728720C= , CM000667.2:g.90728720C=	GRCh38
NC_000005.9:g.90024537C= , CM000667.1:g.90024537C=	GRCh37
NC_000005.8:g.90060293C=	NCBI36
NG_007083.1:g.174921C=
NG_007083.2:g.204377C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10213C= MANE Select	NP_115495.3:p.Arg3405=
ENST00000405460.9:c.10213C= MANE Select	ENSP00000384582.2:p.Arg3405=
NM_032119.3:c.10213C=	NP_115495.3:p.Arg3405=
NR_003149.1:n.10226C=
NR_003149.2:n.10229C=
ENST00000405460.6:c.10213C=	ENSP00000384582.2:p.Arg3405=
ENST00000509621.1:c.2910C=
ENST00000639431.1:c.265+52511C=	ENSP00000491057.1:n.265+52511C=
ENST00000640374.1:n.3357C=
ENST00000640464.1:n.632C=
XM_011543675.1:c.10210C=	XP_011541977.1:p.Arg3404=
XM_011543676.1:c.10132C=	XP_011541978.1:p.Arg3378=
XM_011543677.1:c.7516C=	XP_011541979.1:p.Arg2506=
XM_011543678.1:c.10213C=	XP_011541980.1:p.Arg3405=
XM_011543679.1:c.10213C=	XP_011541981.1:p.Arg3405=
XM_017009963.2:c.10234C=	XP_016865452.1:p.Arg3412=
XM_017009964.2:c.10231C=	XP_016865453.1:p.Arg3411=
XM_017009965.1:c.10231C=	XP_016865454.1:p.Arg3411=
XM_017009966.2:c.10153C=	XP_016865455.1:p.Arg3385=
XM_017009967.1:c.10138C=	XP_016865456.1:p.Arg3380=
XM_017009968.2:c.10234C=	XP_016865457.1:p.Arg3412=
XM_017009969.2:c.10234C=	XP_016865458.1:p.Arg3412=
XM_017009970.2:c.10234C=	XP_016865459.1:p.Arg3412=
XM_017009971.2:c.10234C=	XP_016865460.1:p.Arg3412=
XM_017009972.1:c.3352C=	XP_016865461.1:p.Arg1118=
XM_017009973.1:c.3331C=	XP_016865462.1:p.Arg1111=
XM_017009974.2:c.10234C=	XP_016865463.1:p.Arg3412=
XR_001742802.1:n.2522+12187G=
XR_948560.1:n.271+12187G=