Canonical Allele Identifier: CA1562882058

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745598G= , CM000667.2:g.90745598G=	GRCh38
NC_000005.9:g.90041415G= , CM000667.1:g.90041415G=	GRCh37
NC_000005.8:g.90077171G=	NCBI36
NG_007083.1:g.191799G=
NG_007083.2:g.221255G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10777G= MANE Select	ENSP00000384582.2:p.Glu3593=
ENST00000639431.1:c.265+69389G=	ENSP00000491057.1:n.265+69389G=
ENST00000640374.1:n.3921G=
ENST00000640464.1:n.1196G=
ENST00000405460.6:c.10777G=	ENSP00000384582.2:p.Glu3593=
ENST00000509621.1:c.3474G=
NM_032119.3:c.10777G=	NP_115495.3:p.Glu3593=
NR_003149.1:n.10790G=
XM_011543675.1:c.10774G=	XP_011541977.1:p.Glu3592=
XM_011543676.1:c.10696G=	XP_011541978.1:p.Glu3566=
XM_011543677.1:c.8080G=	XP_011541979.1:p.Glu2694=
XM_011543678.1:c.10777G=	XP_011541980.1:p.Glu3593=
XM_011543679.1:c.10772G=	XP_011541981.1:p.Ter3591=
NM_032119.4:c.10777G= MANE Select	NP_115495.3:p.Glu3593=
XM_017009963.2:c.10798G=	XP_016865452.1:p.Glu3600=
XM_017009964.2:c.10795G=	XP_016865453.1:p.Glu3599=
XM_017009965.1:c.10795G=	XP_016865454.1:p.Glu3599=
XM_017009966.2:c.10717G=	XP_016865455.1:p.Glu3573=
XM_017009967.1:c.10702G=	XP_016865456.1:p.Glu3568=
XM_017009968.2:c.10798G=	XP_016865457.1:p.Glu3600=
XM_017009969.2:c.10798G=	XP_016865458.1:p.Glu3600=
XM_017009970.2:c.10798G=	XP_016865459.1:p.Glu3600=
XM_017009971.2:c.10798G=	XP_016865460.1:p.Glu3600=
XM_017009972.1:c.3916G=	XP_016865461.1:p.Glu1306=
XM_017009973.1:c.3895G=	XP_016865462.1:p.Glu1299=
XM_017009974.2:c.10793G=	XP_016865463.1:p.Ter3598=
NR_003149.2:n.10793G=