Canonical Allele Identifier: CA1562859320

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692762G= , CM000667.2:g.90692762G=	GRCh38
NC_000005.9:g.89988579G= , CM000667.1:g.89988579G=	GRCh37
NC_000005.8:g.90024335G=	NCBI36
NG_007083.1:g.138963G=
NG_007083.2:g.168419G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7109G= MANE Select	ENSP00000384582.2:p.Cys2370=
ENST00000639431.1:c.265+16553G=	ENSP00000491057.1:n.265+16553G=
ENST00000639473.1:n.2568G=
ENST00000640012.1:c.916G=
ENST00000640374.1:n.253G=
ENST00000640403.1:c.4400G=	ENSP00000492531.1:p.Cys1467=
ENST00000640779.1:c.1838G=
ENST00000405460.6:c.7109G=	ENSP00000384582.2:p.Cys2370=
NM_032119.3:c.7109G=	NP_115495.3:p.Cys2370=
NR_003149.1:n.7122G=
XM_011543675.1:c.7106G=	XP_011541977.1:p.Cys2369=
XM_011543676.1:c.7028G=	XP_011541978.1:p.Cys2343=
XM_011543677.1:c.4412G=	XP_011541979.1:p.Cys1471=
XM_011543678.1:c.7109G=	XP_011541980.1:p.Cys2370=
XM_011543679.1:c.7109G=	XP_011541981.1:p.Cys2370=
NM_032119.4:c.7109G= MANE Select	NP_115495.3:p.Cys2370=
XM_017009963.2:c.7109G=	XP_016865452.1:p.Cys2370=
XM_017009964.2:c.7106G=	XP_016865453.1:p.Cys2369=
XM_017009965.1:c.7106G=	XP_016865454.1:p.Cys2369=
XM_017009966.2:c.7028G=	XP_016865455.1:p.Cys2343=
XM_017009967.1:c.7013G=	XP_016865456.1:p.Cys2338=
XM_017009968.2:c.7109G=	XP_016865457.1:p.Cys2370=
XM_017009969.2:c.7109G=	XP_016865458.1:p.Cys2370=
XM_017009970.2:c.7109G=	XP_016865459.1:p.Cys2370=
XM_017009971.2:c.7109G=	XP_016865460.1:p.Cys2370=
XM_017009972.1:c.227G=	XP_016865461.1:p.Cys76=
XM_017009973.1:c.227G=	XP_016865462.1:p.Cys76=
XM_017009974.2:c.7109G=	XP_016865463.1:p.Cys2370=
NR_003149.2:n.7125G=