Canonical Allele Identifier: CA1562855158

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684068T= , CM000667.2:g.90684068T=	GRCh38
NC_000005.9:g.89979885T= , CM000667.1:g.89979885T=	GRCh37
NC_000005.8:g.90015641T=	NCBI36
NG_007083.1:g.130269T=
NG_007083.2:g.159725T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6147T= MANE Select	ENSP00000384582.2:p.Phe2049=
ENST00000639431.1:c.265+7859T=	ENSP00000491057.1:n.265+7859T=
ENST00000639473.1:n.1606T=
ENST00000640012.1:c.165-1712T=
ENST00000640403.1:c.3438T=	ENSP00000492531.1:p.Phe1146=
ENST00000640779.1:c.959T=
ENST00000405460.6:c.6147T=	ENSP00000384582.2:p.Phe2049=
NM_032119.3:c.6147T=	NP_115495.3:p.Phe2049=
NR_003149.1:n.6243T=
XM_011543675.1:c.6144T=	XP_011541977.1:p.Phe2048=
XM_011543676.1:c.6066T=	XP_011541978.1:p.Phe2022=
XM_011543677.1:c.3450T=	XP_011541979.1:p.Phe1150=
XM_011543678.1:c.6147T=	XP_011541980.1:p.Phe2049=
XM_011543679.1:c.6147T=	XP_011541981.1:p.Phe2049=
NM_032119.4:c.6147T= MANE Select	NP_115495.3:p.Phe2049=
XM_017009963.2:c.6147T=	XP_016865452.1:p.Phe2049=
XM_017009964.2:c.6144T=	XP_016865453.1:p.Phe2048=
XM_017009965.1:c.6144T=	XP_016865454.1:p.Phe2048=
XM_017009966.2:c.6066T=	XP_016865455.1:p.Phe2022=
XM_017009967.1:c.6051T=	XP_016865456.1:p.Phe2017=
XM_017009968.2:c.6147T=	XP_016865457.1:p.Phe2049=
XM_017009969.2:c.6147T=	XP_016865458.1:p.Phe2049=
XM_017009970.2:c.6147T=	XP_016865459.1:p.Phe2049=
XM_017009971.2:c.6147T=	XP_016865460.1:p.Phe2049=
XM_017009973.1:c.-653T=	XP_016865462.1:n.-653T=
XM_017009974.2:c.6147T=	XP_016865463.1:p.Phe2049=
NR_003149.2:n.6246T=