Canonical Allele Identifier: CA1562882068

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745618T= , CM000667.2:g.90745618T=	GRCh38
NC_000005.9:g.90041435T= , CM000667.1:g.90041435T=	GRCh37
NC_000005.8:g.90077191T=	NCBI36
NG_007083.1:g.191819T=
NG_007083.2:g.221275T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10797T= MANE Select	ENSP00000384582.2:p.Gly3599=
ENST00000639431.1:c.265+69409T=	ENSP00000491057.1:n.265+69409T=
ENST00000640374.1:n.3941T=
ENST00000640464.1:n.1216T=
ENST00000405460.6:c.10797T=	ENSP00000384582.2:p.Gly3599=
ENST00000509621.1:c.3494T=
NM_032119.3:c.10797T=	NP_115495.3:p.Gly3599=
NR_003149.1:n.10810T=
XM_011543675.1:c.10794T=	XP_011541977.1:p.Gly3598=
XM_011543676.1:c.10716T=	XP_011541978.1:p.Gly3572=
XM_011543677.1:c.8100T=	XP_011541979.1:p.Gly2700=
XM_011543678.1:c.10797T=	XP_011541980.1:p.Gly3599=
XM_011543679.1:c.*19T=	XP_011541981.1:n.*19T=
NM_032119.4:c.10797T= MANE Select	NP_115495.3:p.Gly3599=
XM_017009963.2:c.10818T=	XP_016865452.1:p.Gly3606=
XM_017009964.2:c.10815T=	XP_016865453.1:p.Gly3605=
XM_017009965.1:c.10815T=	XP_016865454.1:p.Gly3605=
XM_017009966.2:c.10737T=	XP_016865455.1:p.Gly3579=
XM_017009967.1:c.10722T=	XP_016865456.1:p.Gly3574=
XM_017009968.2:c.10818T=	XP_016865457.1:p.Gly3606=
XM_017009969.2:c.10818T=	XP_016865458.1:p.Gly3606=
XM_017009970.2:c.10818T=	XP_016865459.1:p.Gly3606=
XM_017009971.2:c.10818T=	XP_016865460.1:p.Gly3606=
XM_017009972.1:c.3936T=	XP_016865461.1:p.Gly1312=
XM_017009973.1:c.3915T=	XP_016865462.1:p.Gly1305=
XM_017009974.2:c.*19T=	XP_016865463.1:n.*19T=
NR_003149.2:n.10813T=