Canonical Allele Identifier: CA1562859398

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692962C= , CM000667.2:g.90692962C=	GRCh38
NC_000005.9:g.89988779C= , CM000667.1:g.89988779C=	GRCh37
NC_000005.8:g.90024535C=	NCBI36
NG_007083.1:g.139163C=
NG_007083.2:g.168619C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7133+176C= MANE Select	ENSP00000384582.2:n.7133+176C=
ENST00000639431.1:c.265+16753C=	ENSP00000491057.1:n.265+16753C=
ENST00000639473.1:n.2592+176C=
ENST00000640012.1:c.940+176C=
ENST00000640374.1:n.277+176C=
ENST00000640403.1:c.4424+176C=	ENSP00000492531.1:n.4424+176C=
ENST00000640779.1:c.1862+176C=
ENST00000405460.6:c.7133+176C=	ENSP00000384582.2:n.7133+176C=
NM_032119.3:c.7133+176C=	NP_115495.3:n.7133+176C=
NR_003149.1:n.7146+176C=
XM_011543675.1:c.7130+176C=	XP_011541977.1:n.7130+176C=
XM_011543676.1:c.7052+176C=	XP_011541978.1:n.7052+176C=
XM_011543677.1:c.4436+176C=	XP_011541979.1:n.4436+176C=
XM_011543678.1:c.7133+176C=	XP_011541980.1:n.7133+176C=
XM_011543679.1:c.7133+176C=	XP_011541981.1:n.7133+176C=
NM_032119.4:c.7133+176C= MANE Select	NP_115495.3:n.7133+176C=
XM_017009963.2:c.7133+176C=	XP_016865452.1:n.7133+176C=
XM_017009964.2:c.7130+176C=	XP_016865453.1:n.7130+176C=
XM_017009965.1:c.7130+176C=	XP_016865454.1:n.7130+176C=
XM_017009966.2:c.7052+176C=	XP_016865455.1:n.7052+176C=
XM_017009967.1:c.7037+176C=	XP_016865456.1:n.7037+176C=
XM_017009968.2:c.7133+176C=	XP_016865457.1:n.7133+176C=
XM_017009969.2:c.7133+176C=	XP_016865458.1:n.7133+176C=
XM_017009970.2:c.7133+176C=	XP_016865459.1:n.7133+176C=
XM_017009971.2:c.7133+176C=	XP_016865460.1:n.7133+176C=
XM_017009972.1:c.251+176C=	XP_016865461.1:n.251+176C=
XM_017009973.1:c.251+176C=	XP_016865462.1:n.251+176C=
XM_017009974.2:c.7133+176C=	XP_016865463.1:n.7133+176C=
NR_003149.2:n.7149+176C=