Canonical Allele Identifier: CA1562895825

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90776521A= , CM000667.2:g.90776521A=	GRCh38
NC_000005.9:g.90072338A= , CM000667.1:g.90072338A=	GRCh37
NC_000005.8:g.90108094A=	NCBI36
NG_007083.1:g.222722A=
NG_007083.2:g.252178A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.12472A= MANE Select	ENSP00000384582.2:p.Arg4158=
ENST00000425867.3:c.1426A=	ENSP00000392618.3:p.Arg476=
ENST00000639431.1:c.265+100312A=	ENSP00000491057.1:n.265+100312A=
ENST00000640464.1:n.2891A=
ENST00000640729.1:n.1049A=
ENST00000405460.6:c.12472A=	ENSP00000384582.2:p.Arg4158=
NM_032119.3:c.12472A=	NP_115495.3:p.Arg4158=
NR_003149.1:n.12485A=
XM_011543675.1:c.12469A=	XP_011541977.1:p.Arg4157=
XM_011543676.1:c.12391A=	XP_011541978.1:p.Arg4131=
XM_011543677.1:c.9775A=	XP_011541979.1:p.Arg3259=
XM_011543678.1:c.12472A=	XP_011541980.1:p.Arg4158=
NM_032119.4:c.12472A= MANE Select	NP_115495.3:p.Arg4158=
XM_017009963.2:c.12493A=	XP_016865452.1:p.Arg4165=
XM_017009964.2:c.12490A=	XP_016865453.1:p.Arg4164=
XM_017009965.1:c.12490A=	XP_016865454.1:p.Arg4164=
XM_017009966.2:c.12412A=	XP_016865455.1:p.Arg4138=
XM_017009967.1:c.12397A=	XP_016865456.1:p.Arg4133=
XM_017009968.2:c.12493A=	XP_016865457.1:p.Arg4165=
XM_017009969.2:c.12493A=	XP_016865458.1:p.Arg4165=
XM_017009970.2:c.12493A=	XP_016865459.1:p.Arg4165=
XM_017009971.2:c.12493A=	XP_016865460.1:p.Arg4165=
XM_017009972.1:c.5611A=	XP_016865461.1:p.Arg1871=
XM_017009973.1:c.5590A=	XP_016865462.1:p.Arg1864=
NR_003149.2:n.12488A=