Canonical Allele Identifier: CA1562859280

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692684C= , CM000667.2:g.90692684C=	GRCh38
NC_000005.9:g.89988501C= , CM000667.1:g.89988501C=	GRCh37
NC_000005.8:g.90024257C=	NCBI36
NG_007083.1:g.138885C=
NG_007083.2:g.168341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7031C= MANE Select	ENSP00000384582.2:p.Ala2344=
ENST00000639431.1:c.265+16475C=	ENSP00000491057.1:n.265+16475C=
ENST00000639473.1:n.2490C=
ENST00000640012.1:c.838C=
ENST00000640374.1:n.175C=
ENST00000640403.1:c.4322C=	ENSP00000492531.1:p.Ala1441=
ENST00000640779.1:c.1760C=
ENST00000405460.6:c.7031C=	ENSP00000384582.2:p.Ala2344=
NM_032119.3:c.7031C=	NP_115495.3:p.Ala2344=
NR_003149.1:n.7044C=
XM_011543675.1:c.7028C=	XP_011541977.1:p.Ala2343=
XM_011543676.1:c.6950C=	XP_011541978.1:p.Ala2317=
XM_011543677.1:c.4334C=	XP_011541979.1:p.Ala1445=
XM_011543678.1:c.7031C=	XP_011541980.1:p.Ala2344=
XM_011543679.1:c.7031C=	XP_011541981.1:p.Ala2344=
NM_032119.4:c.7031C= MANE Select	NP_115495.3:p.Ala2344=
XM_017009963.2:c.7031C=	XP_016865452.1:p.Ala2344=
XM_017009964.2:c.7028C=	XP_016865453.1:p.Ala2343=
XM_017009965.1:c.7028C=	XP_016865454.1:p.Ala2343=
XM_017009966.2:c.6950C=	XP_016865455.1:p.Ala2317=
XM_017009967.1:c.6935C=	XP_016865456.1:p.Ala2312=
XM_017009968.2:c.7031C=	XP_016865457.1:p.Ala2344=
XM_017009969.2:c.7031C=	XP_016865458.1:p.Ala2344=
XM_017009970.2:c.7031C=	XP_016865459.1:p.Ala2344=
XM_017009971.2:c.7031C=	XP_016865460.1:p.Ala2344=
XM_017009972.1:c.149C=	XP_016865461.1:p.Ala50=
XM_017009973.1:c.149C=	XP_016865462.1:p.Ala50=
XM_017009974.2:c.7031C=	XP_016865463.1:p.Ala2344=
NR_003149.2:n.7047C=