Canonical Allele Identifier: CA1562908488

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810997G= , CM000667.2:g.90810997G=	GRCh38
NC_000005.9:g.90106814G= , CM000667.1:g.90106814G=	GRCh37
NC_000005.8:g.90142570G=	NCBI36
NG_007083.1:g.257198G=
NG_007083.2:g.286654G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15737G= MANE Select	ENSP00000384582.2:p.Arg5246=
ENST00000425867.3:c.4691G=	ENSP00000392618.3:p.Arg1564=
ENST00000638510.1:n.3004G=
ENST00000639431.1:c.265+134788G=	ENSP00000491057.1:n.265+134788G=
ENST00000640407.1:c.2147G=	ENSP00000491425.1:p.Arg716=
ENST00000405460.6:c.15737G=	ENSP00000384582.2:p.Arg5246=
ENST00000425867.2:c.2720G=	ENSP00000392618.2:p.Arg907=
NM_032119.3:c.15737G=	NP_115495.3:p.Arg5246=
NR_003149.1:n.15750G=
XM_011543675.1:c.15734G=	XP_011541977.1:p.Arg5245=
XM_011543676.1:c.15656G=	XP_011541978.1:p.Arg5219=
XM_011543677.1:c.13040G=	XP_011541979.1:p.Arg4347=
NM_032119.4:c.15737G= MANE Select	NP_115495.3:p.Arg5246=
XM_017009963.2:c.15758G=	XP_016865452.1:p.Arg5253=
XM_017009964.2:c.15755G=	XP_016865453.1:p.Arg5252=
XM_017009965.1:c.15755G=	XP_016865454.1:p.Arg5252=
XM_017009966.2:c.15677G=	XP_016865455.1:p.Arg5226=
XM_017009967.1:c.15662G=	XP_016865456.1:p.Arg5221=
XM_017009968.2:c.15578G=	XP_016865457.1:p.Arg5193=
XM_017009969.2:c.15758G=	XP_016865458.1:p.Arg5253=
XM_017009972.1:c.8876G=	XP_016865461.1:p.Arg2959=
XM_017009973.1:c.8855G=	XP_016865462.1:p.Arg2952=
NR_003149.2:n.15753G=