Canonical Allele Identifier: CA1562882059

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745601C= , CM000667.2:g.90745601C=	GRCh38
NC_000005.9:g.90041418C= , CM000667.1:g.90041418C=	GRCh37
NC_000005.8:g.90077174C=	NCBI36
NG_007083.1:g.191802C=
NG_007083.2:g.221258C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10780C= MANE Select	ENSP00000384582.2:p.Leu3594=
ENST00000639431.1:c.265+69392C=	ENSP00000491057.1:n.265+69392C=
ENST00000640374.1:n.3924C=
ENST00000640464.1:n.1199C=
ENST00000405460.6:c.10780C=	ENSP00000384582.2:p.Leu3594=
ENST00000509621.1:c.3477C=
NM_032119.3:c.10780C=	NP_115495.3:p.Leu3594=
NR_003149.1:n.10793C=
XM_011543675.1:c.10777C=	XP_011541977.1:p.Leu3593=
XM_011543676.1:c.10699C=	XP_011541978.1:p.Leu3567=
XM_011543677.1:c.8083C=	XP_011541979.1:p.Leu2695=
XM_011543678.1:c.10780C=	XP_011541980.1:p.Leu3594=
XM_011543679.1:c.*2C=	XP_011541981.1:n.*2C=
NM_032119.4:c.10780C= MANE Select	NP_115495.3:p.Leu3594=
XM_017009963.2:c.10801C=	XP_016865452.1:p.Leu3601=
XM_017009964.2:c.10798C=	XP_016865453.1:p.Leu3600=
XM_017009965.1:c.10798C=	XP_016865454.1:p.Leu3600=
XM_017009966.2:c.10720C=	XP_016865455.1:p.Leu3574=
XM_017009967.1:c.10705C=	XP_016865456.1:p.Leu3569=
XM_017009968.2:c.10801C=	XP_016865457.1:p.Leu3601=
XM_017009969.2:c.10801C=	XP_016865458.1:p.Leu3601=
XM_017009970.2:c.10801C=	XP_016865459.1:p.Leu3601=
XM_017009971.2:c.10801C=	XP_016865460.1:p.Leu3601=
XM_017009972.1:c.3919C=	XP_016865461.1:p.Leu1307=
XM_017009973.1:c.3898C=	XP_016865462.1:p.Leu1300=
XM_017009974.2:c.*2C=	XP_016865463.1:n.*2C=
NR_003149.2:n.10796C=