Canonical Allele Identifier: CA1562882088

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745663T= , CM000667.2:g.90745663T=	GRCh38
NC_000005.9:g.90041480T= , CM000667.1:g.90041480T=	GRCh37
NC_000005.8:g.90077236T=	NCBI36
NG_007083.1:g.191864T=
NG_007083.2:g.221320T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10842T= MANE Select	ENSP00000384582.2:p.Val3614=
ENST00000639431.1:c.265+69454T=	ENSP00000491057.1:n.265+69454T=
ENST00000640374.1:n.3986T=
ENST00000640464.1:n.1261T=
ENST00000405460.6:c.10842T=	ENSP00000384582.2:p.Val3614=
ENST00000509621.1:c.3539T=
NM_032119.3:c.10842T=	NP_115495.3:p.Val3614=
NR_003149.1:n.10855T=
XM_011543675.1:c.10839T=	XP_011541977.1:p.Val3613=
XM_011543676.1:c.10761T=	XP_011541978.1:p.Val3587=
XM_011543677.1:c.8145T=	XP_011541979.1:p.Val2715=
XM_011543678.1:c.10842T=	XP_011541980.1:p.Val3614=
XM_011543679.1:c.*64T=	XP_011541981.1:n.*64T=
NM_032119.4:c.10842T= MANE Select	NP_115495.3:p.Val3614=
XM_017009963.2:c.10863T=	XP_016865452.1:p.Val3621=
XM_017009964.2:c.10860T=	XP_016865453.1:p.Val3620=
XM_017009965.1:c.10860T=	XP_016865454.1:p.Val3620=
XM_017009966.2:c.10782T=	XP_016865455.1:p.Val3594=
XM_017009967.1:c.10767T=	XP_016865456.1:p.Val3589=
XM_017009968.2:c.10863T=	XP_016865457.1:p.Val3621=
XM_017009969.2:c.10863T=	XP_016865458.1:p.Val3621=
XM_017009970.2:c.10863T=	XP_016865459.1:p.Val3621=
XM_017009971.2:c.10863T=	XP_016865460.1:p.Val3621=
XM_017009972.1:c.3981T=	XP_016865461.1:p.Val1327=
XM_017009973.1:c.3960T=	XP_016865462.1:p.Val1320=
XM_017009974.2:c.*64T=	XP_016865463.1:n.*64T=
NR_003149.2:n.10858T=