Canonical Allele Identifier: CA1562908479

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810996C= , CM000667.2:g.90810996C=	GRCh38
NC_000005.9:g.90106813C= , CM000667.1:g.90106813C=	GRCh37
NC_000005.8:g.90142569C=	NCBI36
NG_007083.1:g.257197C=
NG_007083.2:g.286653C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15736C= MANE Select	ENSP00000384582.2:p.Arg5246=
ENST00000425867.3:c.4690C=	ENSP00000392618.3:p.Arg1564=
ENST00000638510.1:n.3003C=
ENST00000639431.1:c.265+134787C=	ENSP00000491057.1:n.265+134787C=
ENST00000640407.1:c.2146C=	ENSP00000491425.1:p.Arg716=
ENST00000405460.6:c.15736C=	ENSP00000384582.2:p.Arg5246=
ENST00000425867.2:c.2719C=	ENSP00000392618.2:p.Arg907=
NM_032119.3:c.15736C=	NP_115495.3:p.Arg5246=
NR_003149.1:n.15749C=
XM_011543675.1:c.15733C=	XP_011541977.1:p.Arg5245=
XM_011543676.1:c.15655C=	XP_011541978.1:p.Arg5219=
XM_011543677.1:c.13039C=	XP_011541979.1:p.Arg4347=
NM_032119.4:c.15736C= MANE Select	NP_115495.3:p.Arg5246=
XM_017009963.2:c.15757C=	XP_016865452.1:p.Arg5253=
XM_017009964.2:c.15754C=	XP_016865453.1:p.Arg5252=
XM_017009965.1:c.15754C=	XP_016865454.1:p.Arg5252=
XM_017009966.2:c.15676C=	XP_016865455.1:p.Arg5226=
XM_017009967.1:c.15661C=	XP_016865456.1:p.Arg5221=
XM_017009968.2:c.15577C=	XP_016865457.1:p.Arg5193=
XM_017009969.2:c.15757C=	XP_016865458.1:p.Arg5253=
XM_017009972.1:c.8875C=	XP_016865461.1:p.Arg2959=
XM_017009973.1:c.8854C=	XP_016865462.1:p.Arg2952=
NR_003149.2:n.15752C=