Canonical Allele Identifier: CA1562882096

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745685A= , CM000667.2:g.90745685A=	GRCh38
NC_000005.9:g.90041502A= , CM000667.1:g.90041502A=	GRCh37
NC_000005.8:g.90077258A=	NCBI36
NG_007083.1:g.191886A=
NG_007083.2:g.221342A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10864A= MANE Select	ENSP00000384582.2:p.Lys3622=
ENST00000639431.1:c.265+69476A=	ENSP00000491057.1:n.265+69476A=
ENST00000640374.1:n.4008A=
ENST00000640464.1:n.1283A=
ENST00000405460.6:c.10864A=	ENSP00000384582.2:p.Lys3622=
ENST00000509621.1:c.3561A=
NM_032119.3:c.10864A=	NP_115495.3:p.Lys3622=
NR_003149.1:n.10877A=
XM_011543675.1:c.10861A=	XP_011541977.1:p.Lys3621=
XM_011543676.1:c.10783A=	XP_011541978.1:p.Lys3595=
XM_011543677.1:c.8167A=	XP_011541979.1:p.Lys2723=
XM_011543678.1:c.10864A=	XP_011541980.1:p.Lys3622=
XM_011543679.1:c.*86A=	XP_011541981.1:n.*86A=
NM_032119.4:c.10864A= MANE Select	NP_115495.3:p.Lys3622=
XM_017009963.2:c.10885A=	XP_016865452.1:p.Lys3629=
XM_017009964.2:c.10882A=	XP_016865453.1:p.Lys3628=
XM_017009965.1:c.10882A=	XP_016865454.1:p.Lys3628=
XM_017009966.2:c.10804A=	XP_016865455.1:p.Lys3602=
XM_017009967.1:c.10789A=	XP_016865456.1:p.Lys3597=
XM_017009968.2:c.10885A=	XP_016865457.1:p.Lys3629=
XM_017009969.2:c.10885A=	XP_016865458.1:p.Lys3629=
XM_017009970.2:c.10885A=	XP_016865459.1:p.Lys3629=
XM_017009971.2:c.10885A=	XP_016865460.1:p.Lys3629=
XM_017009972.1:c.4003A=	XP_016865461.1:p.Lys1335=
XM_017009973.1:c.3982A=	XP_016865462.1:p.Lys1328=
XM_017009974.2:c.*86A=	XP_016865463.1:n.*86A=
NR_003149.2:n.10880A=