Canonical Allele Identifier: CA1562859406

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692978T= , CM000667.2:g.90692978T=	GRCh38
NC_000005.9:g.89988795T= , CM000667.1:g.89988795T=	GRCh37
NC_000005.8:g.90024551T=	NCBI36
NG_007083.1:g.139179T=
NG_007083.2:g.168635T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7133+192T= MANE Select	ENSP00000384582.2:n.7133+192T=
ENST00000639431.1:c.265+16769T=	ENSP00000491057.1:n.265+16769T=
ENST00000639473.1:n.2592+192T=
ENST00000640012.1:c.940+192T=
ENST00000640374.1:n.277+192T=
ENST00000640403.1:c.4424+192T=	ENSP00000492531.1:n.4424+192T=
ENST00000640779.1:c.1862+192T=
ENST00000405460.6:c.7133+192T=	ENSP00000384582.2:n.7133+192T=
NM_032119.3:c.7133+192T=	NP_115495.3:n.7133+192T=
NR_003149.1:n.7146+192T=
XM_011543675.1:c.7130+192T=	XP_011541977.1:n.7130+192T=
XM_011543676.1:c.7052+192T=	XP_011541978.1:n.7052+192T=
XM_011543677.1:c.4436+192T=	XP_011541979.1:n.4436+192T=
XM_011543678.1:c.7133+192T=	XP_011541980.1:n.7133+192T=
XM_011543679.1:c.7133+192T=	XP_011541981.1:n.7133+192T=
NM_032119.4:c.7133+192T= MANE Select	NP_115495.3:n.7133+192T=
XM_017009963.2:c.7133+192T=	XP_016865452.1:n.7133+192T=
XM_017009964.2:c.7130+192T=	XP_016865453.1:n.7130+192T=
XM_017009965.1:c.7130+192T=	XP_016865454.1:n.7130+192T=
XM_017009966.2:c.7052+192T=	XP_016865455.1:n.7052+192T=
XM_017009967.1:c.7037+192T=	XP_016865456.1:n.7037+192T=
XM_017009968.2:c.7133+192T=	XP_016865457.1:n.7133+192T=
XM_017009969.2:c.7133+192T=	XP_016865458.1:n.7133+192T=
XM_017009970.2:c.7133+192T=	XP_016865459.1:n.7133+192T=
XM_017009971.2:c.7133+192T=	XP_016865460.1:n.7133+192T=
XM_017009972.1:c.251+192T=	XP_016865461.1:n.251+192T=
XM_017009973.1:c.251+192T=	XP_016865462.1:n.251+192T=
XM_017009974.2:c.7133+192T=	XP_016865463.1:n.7133+192T=
NR_003149.2:n.7149+192T=