Canonical Allele Identifier: CA1562886224

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755141A= , CM000667.2:g.90755141A=	GRCh38
NC_000005.9:g.90050958A= , CM000667.1:g.90050958A=	GRCh37
NC_000005.8:g.90086714A=	NCBI36
NG_007083.1:g.201342A=
NG_007083.2:g.230798A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11536A= MANE Select	ENSP00000384582.2:p.Lys3846=
ENST00000425867.3:c.667A=	ENSP00000392618.3:p.Lys223=
ENST00000639431.1:c.265+78932A=	ENSP00000491057.1:n.265+78932A=
ENST00000640374.1:n.4680A=
ENST00000640464.1:n.1955A=
ENST00000405460.6:c.11536A=	ENSP00000384582.2:p.Lys3846=
ENST00000509621.1:c.4233A=
NM_032119.3:c.11536A=	NP_115495.3:p.Lys3846=
NR_003149.1:n.11549A=
XM_011543675.1:c.11533A=	XP_011541977.1:p.Lys3845=
XM_011543676.1:c.11455A=	XP_011541978.1:p.Lys3819=
XM_011543677.1:c.8839A=	XP_011541979.1:p.Lys2947=
XM_011543678.1:c.11536A=	XP_011541980.1:p.Lys3846=
NM_032119.4:c.11536A= MANE Select	NP_115495.3:p.Lys3846=
XM_017009963.2:c.11557A=	XP_016865452.1:p.Lys3853=
XM_017009964.2:c.11554A=	XP_016865453.1:p.Lys3852=
XM_017009965.1:c.11554A=	XP_016865454.1:p.Lys3852=
XM_017009966.2:c.11476A=	XP_016865455.1:p.Lys3826=
XM_017009967.1:c.11461A=	XP_016865456.1:p.Lys3821=
XM_017009968.2:c.11557A=	XP_016865457.1:p.Lys3853=
XM_017009969.2:c.11557A=	XP_016865458.1:p.Lys3853=
XM_017009970.2:c.11557A=	XP_016865459.1:p.Lys3853=
XM_017009971.2:c.11557A=	XP_016865460.1:p.Lys3853=
XM_017009972.1:c.4675A=	XP_016865461.1:p.Lys1559=
XM_017009973.1:c.4654A=	XP_016865462.1:p.Lys1552=
NR_003149.2:n.11552A=