Canonical Allele Identifier: CA1562855156

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684063C= , CM000667.2:g.90684063C=	GRCh38
NC_000005.9:g.89979880C= , CM000667.1:g.89979880C=	GRCh37
NC_000005.8:g.90015636C=	NCBI36
NG_007083.1:g.130264C=
NG_007083.2:g.159720C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6142C= MANE Select	ENSP00000384582.2:p.Leu2048=
ENST00000639431.1:c.265+7854C=	ENSP00000491057.1:n.265+7854C=
ENST00000639473.1:n.1601C=
ENST00000640012.1:c.165-1717C=
ENST00000640403.1:c.3433C=	ENSP00000492531.1:p.Leu1145=
ENST00000640779.1:c.954C=
ENST00000405460.6:c.6142C=	ENSP00000384582.2:p.Leu2048=
NM_032119.3:c.6142C=	NP_115495.3:p.Leu2048=
NR_003149.1:n.6238C=
XM_011543675.1:c.6139C=	XP_011541977.1:p.Leu2047=
XM_011543676.1:c.6061C=	XP_011541978.1:p.Leu2021=
XM_011543677.1:c.3445C=	XP_011541979.1:p.Leu1149=
XM_011543678.1:c.6142C=	XP_011541980.1:p.Leu2048=
XM_011543679.1:c.6142C=	XP_011541981.1:p.Leu2048=
NM_032119.4:c.6142C= MANE Select	NP_115495.3:p.Leu2048=
XM_017009963.2:c.6142C=	XP_016865452.1:p.Leu2048=
XM_017009964.2:c.6139C=	XP_016865453.1:p.Leu2047=
XM_017009965.1:c.6139C=	XP_016865454.1:p.Leu2047=
XM_017009966.2:c.6061C=	XP_016865455.1:p.Leu2021=
XM_017009967.1:c.6046C=	XP_016865456.1:p.Leu2016=
XM_017009968.2:c.6142C=	XP_016865457.1:p.Leu2048=
XM_017009969.2:c.6142C=	XP_016865458.1:p.Leu2048=
XM_017009970.2:c.6142C=	XP_016865459.1:p.Leu2048=
XM_017009971.2:c.6142C=	XP_016865460.1:p.Leu2048=
XM_017009973.1:c.-658C=	XP_016865462.1:n.-658C=
XM_017009974.2:c.6142C=	XP_016865463.1:p.Leu2048=
NR_003149.2:n.6241C=