Canonical Allele Identifier: CA1562918283

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823510G= , CM000667.2:g.90823510G=	GRCh38
NC_000005.9:g.90119327G= , CM000667.1:g.90119327G=	GRCh37
NC_000005.8:g.90155083G=	NCBI36
NG_007083.1:g.269711G=
NG_007083.2:g.299167G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16282G= MANE Select	ENSP00000384582.2:p.Glu5428=
ENST00000425867.3:c.5236G=	ENSP00000392618.3:p.Glu1746=
ENST00000638510.1:n.3549G=
ENST00000639431.1:c.265+147301G=	ENSP00000491057.1:n.265+147301G=
ENST00000640061.1:n.128+1328G=
ENST00000640407.1:c.2692G=	ENSP00000491425.1:p.Glu898=
ENST00000405460.6:c.16282G=	ENSP00000384582.2:p.Glu5428=
ENST00000425867.2:c.3265G=	ENSP00000392618.2:p.Glu1089=
NM_032119.3:c.16282G=	NP_115495.3:p.Glu5428=
NR_003149.1:n.16295G=
XM_011543675.1:c.16279G=	XP_011541977.1:p.Glu5427=
XM_011543676.1:c.16201G=	XP_011541978.1:p.Glu5401=
XM_011543677.1:c.13585G=	XP_011541979.1:p.Glu4529=
NM_032119.4:c.16282G= MANE Select	NP_115495.3:p.Glu5428=
XM_017009963.2:c.16303G=	XP_016865452.1:p.Glu5435=
XM_017009964.2:c.16300G=	XP_016865453.1:p.Glu5434=
XM_017009965.1:c.16300G=	XP_016865454.1:p.Glu5434=
XM_017009966.2:c.16222G=	XP_016865455.1:p.Glu5408=
XM_017009967.1:c.16207G=	XP_016865456.1:p.Glu5403=
XM_017009968.2:c.16123G=	XP_016865457.1:p.Glu5375=
XM_017009969.2:c.16303G=	XP_016865458.1:p.Glu5435=
XM_017009972.1:c.9421G=	XP_016865461.1:p.Glu3141=
XM_017009973.1:c.9400G=	XP_016865462.1:p.Glu3134=
NR_003149.2:n.16298G=