Canonical Allele Identifier: CA1562886237

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755174T= , CM000667.2:g.90755174T=	GRCh38
NC_000005.9:g.90050991T= , CM000667.1:g.90050991T=	GRCh37
NC_000005.8:g.90086747T=	NCBI36
NG_007083.1:g.201375T=
NG_007083.2:g.230831T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11569T= MANE Select	ENSP00000384582.2:p.Ser3857=
ENST00000425867.3:c.700T=	ENSP00000392618.3:p.Ser234=
ENST00000639431.1:c.265+78965T=	ENSP00000491057.1:n.265+78965T=
ENST00000640374.1:n.4713T=
ENST00000640464.1:n.1988T=
ENST00000405460.6:c.11569T=	ENSP00000384582.2:p.Ser3857=
ENST00000509621.1:c.4266T=
NM_032119.3:c.11569T=	NP_115495.3:p.Ser3857=
NR_003149.1:n.11582T=
XM_011543675.1:c.11566T=	XP_011541977.1:p.Ser3856=
XM_011543676.1:c.11488T=	XP_011541978.1:p.Ser3830=
XM_011543677.1:c.8872T=	XP_011541979.1:p.Ser2958=
XM_011543678.1:c.11569T=	XP_011541980.1:p.Ser3857=
NM_032119.4:c.11569T= MANE Select	NP_115495.3:p.Ser3857=
XM_017009963.2:c.11590T=	XP_016865452.1:p.Ser3864=
XM_017009964.2:c.11587T=	XP_016865453.1:p.Ser3863=
XM_017009965.1:c.11587T=	XP_016865454.1:p.Ser3863=
XM_017009966.2:c.11509T=	XP_016865455.1:p.Ser3837=
XM_017009967.1:c.11494T=	XP_016865456.1:p.Ser3832=
XM_017009968.2:c.11590T=	XP_016865457.1:p.Ser3864=
XM_017009969.2:c.11590T=	XP_016865458.1:p.Ser3864=
XM_017009970.2:c.11590T=	XP_016865459.1:p.Ser3864=
XM_017009971.2:c.11590T=	XP_016865460.1:p.Ser3864=
XM_017009972.1:c.4708T=	XP_016865461.1:p.Ser1570=
XM_017009973.1:c.4687T=	XP_016865462.1:p.Ser1563=
NR_003149.2:n.11585T=