Canonical Allele Identifier: CA1562886947

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90756940C= , CM000667.2:g.90756940C=	GRCh38
NC_000005.9:g.90052757C= , CM000667.1:g.90052757C=	GRCh37
NC_000005.8:g.90088513C=	NCBI36
NG_007083.1:g.203141C=
NG_007083.2:g.232597C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11758-39C= MANE Select	ENSP00000384582.2:n.11758-39C=
ENST00000425867.3:c.712-39C=	ENSP00000392618.3:n.712-39C=
ENST00000639431.1:c.265+80731C=	ENSP00000491057.1:n.265+80731C=
ENST00000639884.1:n.373C=
ENST00000640374.1:n.4725-39C=
ENST00000640464.1:n.2177-39C=
ENST00000405460.6:c.11758-39C=	ENSP00000384582.2:n.11758-39C=
ENST00000509621.1:c.4455-39C=
NM_032119.3:c.11758-39C=	NP_115495.3:n.11758-39C=
NR_003149.1:n.11771-39C=
XM_011543675.1:c.11755-39C=	XP_011541977.1:n.11755-39C=
XM_011543676.1:c.11677-39C=	XP_011541978.1:n.11677-39C=
XM_011543677.1:c.9061-39C=	XP_011541979.1:n.9061-39C=
XM_011543678.1:c.11758-39C=	XP_011541980.1:n.11758-39C=
NM_032119.4:c.11758-39C= MANE Select	NP_115495.3:n.11758-39C=
XM_017009963.2:c.11779-39C=	XP_016865452.1:n.11779-39C=
XM_017009964.2:c.11776-39C=	XP_016865453.1:n.11776-39C=
XM_017009965.1:c.11776-39C=	XP_016865454.1:n.11776-39C=
XM_017009966.2:c.11698-39C=	XP_016865455.1:n.11698-39C=
XM_017009967.1:c.11683-39C=	XP_016865456.1:n.11683-39C=
XM_017009968.2:c.11779-39C=	XP_016865457.1:n.11779-39C=
XM_017009969.2:c.11779-39C=	XP_016865458.1:n.11779-39C=
XM_017009970.2:c.11779-39C=	XP_016865459.1:n.11779-39C=
XM_017009971.2:c.11779-39C=	XP_016865460.1:n.11779-39C=
XM_017009972.1:c.4897-39C=	XP_016865461.1:n.4897-39C=
XM_017009973.1:c.4876-39C=	XP_016865462.1:n.4876-39C=
NR_003149.2:n.11774-39C=