Canonical Allele Identifier: CA1562867519

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712295T= , CM000667.2:g.90712295T=	GRCh38
NC_000005.9:g.90008112T= , CM000667.1:g.90008112T=	GRCh37
NC_000005.8:g.90043868T=	NCBI36
NG_007083.1:g.158496T=
NG_007083.2:g.187952T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9051T= MANE Select	ENSP00000384582.2:p.His3017=
ENST00000639431.1:c.265+36086T=	ENSP00000491057.1:n.265+36086T=
ENST00000639473.1:n.4510T=
ENST00000640012.1:c.2858T=
ENST00000640374.1:n.2195T=
ENST00000640779.1:c.3780T=
ENST00000405460.6:c.9051T=	ENSP00000384582.2:p.His3017=
ENST00000509621.1:c.1748T=
NM_032119.3:c.9051T=	NP_115495.3:p.His3017=
NR_003149.1:n.9064T=
XM_011543675.1:c.9048T=	XP_011541977.1:p.His3016=
XM_011543676.1:c.8970T=	XP_011541978.1:p.His2990=
XM_011543677.1:c.6354T=	XP_011541979.1:p.His2118=
XM_011543678.1:c.9051T=	XP_011541980.1:p.His3017=
XM_011543679.1:c.9051T=	XP_011541981.1:p.His3017=
NM_032119.4:c.9051T= MANE Select	NP_115495.3:p.His3017=
XM_017009963.2:c.9072T=	XP_016865452.1:p.His3024=
XM_017009964.2:c.9069T=	XP_016865453.1:p.His3023=
XM_017009965.1:c.9069T=	XP_016865454.1:p.His3023=
XM_017009966.2:c.8991T=	XP_016865455.1:p.His2997=
XM_017009967.1:c.8976T=	XP_016865456.1:p.His2992=
XM_017009968.2:c.9072T=	XP_016865457.1:p.His3024=
XM_017009969.2:c.9072T=	XP_016865458.1:p.His3024=
XM_017009970.2:c.9072T=	XP_016865459.1:p.His3024=
XM_017009971.2:c.9072T=	XP_016865460.1:p.His3024=
XM_017009972.1:c.2190T=	XP_016865461.1:p.His730=
XM_017009973.1:c.2169T=	XP_016865462.1:p.His723=
XM_017009974.2:c.9072T=	XP_016865463.1:p.His3024=
NR_003149.2:n.9067T=