Canonical Allele Identifier: CA1562869761

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720073A= , CM000667.2:g.90720073A=	GRCh38
NC_000005.9:g.90015890A= , CM000667.1:g.90015890A=	GRCh37
NC_000005.8:g.90051646A=	NCBI36
NG_007083.1:g.166274A=
NG_007083.2:g.195730A=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9473A= MANE Select	NP_115495.3:p.Asp3158=
ENST00000405460.9:c.9473A= MANE Select	ENSP00000384582.2:p.Asp3158=
NM_032119.3:c.9473A=	NP_115495.3:p.Asp3158=
NR_003149.1:n.9486A=
NR_003149.2:n.9489A=
ENST00000405460.6:c.9473A=	ENSP00000384582.2:p.Asp3158=
ENST00000509621.1:c.2170A=
ENST00000639431.1:c.265+43864A=	ENSP00000491057.1:n.265+43864A=
ENST00000640374.1:n.2617A=
ENST00000640779.1:c.4202A=
XM_011543675.1:c.9470A=	XP_011541977.1:p.Asp3157=
XM_011543676.1:c.9392A=	XP_011541978.1:p.Asp3131=
XM_011543677.1:c.6776A=	XP_011541979.1:p.Asp2259=
XM_011543678.1:c.9473A=	XP_011541980.1:p.Asp3158=
XM_011543679.1:c.9473A=	XP_011541981.1:p.Asp3158=
XM_017009963.2:c.9494A=	XP_016865452.1:p.Asp3165=
XM_017009964.2:c.9491A=	XP_016865453.1:p.Asp3164=
XM_017009965.1:c.9491A=	XP_016865454.1:p.Asp3164=
XM_017009966.2:c.9413A=	XP_016865455.1:p.Asp3138=
XM_017009967.1:c.9398A=	XP_016865456.1:p.Asp3133=
XM_017009968.2:c.9494A=	XP_016865457.1:p.Asp3165=
XM_017009969.2:c.9494A=	XP_016865458.1:p.Asp3165=
XM_017009970.2:c.9494A=	XP_016865459.1:p.Asp3165=
XM_017009971.2:c.9494A=	XP_016865460.1:p.Asp3165=
XM_017009972.1:c.2612A=	XP_016865461.1:p.Asp871=
XM_017009973.1:c.2591A=	XP_016865462.1:p.Asp864=
XM_017009974.2:c.9494A=	XP_016865463.1:p.Asp3165=
XR_001742802.1:n.2523-4264T=
XR_948560.1:n.272-4264T=