Canonical Allele Identifier: CA1562859297

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692717C= , CM000667.2:g.90692717C=	GRCh38
NC_000005.9:g.89988534C= , CM000667.1:g.89988534C=	GRCh37
NC_000005.8:g.90024290C=	NCBI36
NG_007083.1:g.138918C=
NG_007083.2:g.168374C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7064C= MANE Select	ENSP00000384582.2:p.Ala2355=
ENST00000639431.1:c.265+16508C=	ENSP00000491057.1:n.265+16508C=
ENST00000639473.1:n.2523C=
ENST00000640012.1:c.871C=
ENST00000640374.1:n.208C=
ENST00000640403.1:c.4355C=	ENSP00000492531.1:p.Ala1452=
ENST00000640779.1:c.1793C=
ENST00000405460.6:c.7064C=	ENSP00000384582.2:p.Ala2355=
NM_032119.3:c.7064C=	NP_115495.3:p.Ala2355=
NR_003149.1:n.7077C=
XM_011543675.1:c.7061C=	XP_011541977.1:p.Ala2354=
XM_011543676.1:c.6983C=	XP_011541978.1:p.Ala2328=
XM_011543677.1:c.4367C=	XP_011541979.1:p.Ala1456=
XM_011543678.1:c.7064C=	XP_011541980.1:p.Ala2355=
XM_011543679.1:c.7064C=	XP_011541981.1:p.Ala2355=
NM_032119.4:c.7064C= MANE Select	NP_115495.3:p.Ala2355=
XM_017009963.2:c.7064C=	XP_016865452.1:p.Ala2355=
XM_017009964.2:c.7061C=	XP_016865453.1:p.Ala2354=
XM_017009965.1:c.7061C=	XP_016865454.1:p.Ala2354=
XM_017009966.2:c.6983C=	XP_016865455.1:p.Ala2328=
XM_017009967.1:c.6968C=	XP_016865456.1:p.Ala2323=
XM_017009968.2:c.7064C=	XP_016865457.1:p.Ala2355=
XM_017009969.2:c.7064C=	XP_016865458.1:p.Ala2355=
XM_017009970.2:c.7064C=	XP_016865459.1:p.Ala2355=
XM_017009971.2:c.7064C=	XP_016865460.1:p.Ala2355=
XM_017009972.1:c.182C=	XP_016865461.1:p.Ala61=
XM_017009973.1:c.182C=	XP_016865462.1:p.Ala61=
XM_017009974.2:c.7064C=	XP_016865463.1:p.Ala2355=
NR_003149.2:n.7080C=