Canonical Allele Identifier: CA1562886232

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755167C= , CM000667.2:g.90755167C=	GRCh38
NC_000005.9:g.90050984C= , CM000667.1:g.90050984C=	GRCh37
NC_000005.8:g.90086740C=	NCBI36
NG_007083.1:g.201368C=
NG_007083.2:g.230824C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11562C= MANE Select	ENSP00000384582.2:p.Ala3854=
ENST00000425867.3:c.693C=	ENSP00000392618.3:p.Ala231=
ENST00000639431.1:c.265+78958C=	ENSP00000491057.1:n.265+78958C=
ENST00000640374.1:n.4706C=
ENST00000640464.1:n.1981C=
ENST00000405460.6:c.11562C=	ENSP00000384582.2:p.Ala3854=
ENST00000509621.1:c.4259C=
NM_032119.3:c.11562C=	NP_115495.3:p.Ala3854=
NR_003149.1:n.11575C=
XM_011543675.1:c.11559C=	XP_011541977.1:p.Ala3853=
XM_011543676.1:c.11481C=	XP_011541978.1:p.Ala3827=
XM_011543677.1:c.8865C=	XP_011541979.1:p.Ala2955=
XM_011543678.1:c.11562C=	XP_011541980.1:p.Ala3854=
NM_032119.4:c.11562C= MANE Select	NP_115495.3:p.Ala3854=
XM_017009963.2:c.11583C=	XP_016865452.1:p.Ala3861=
XM_017009964.2:c.11580C=	XP_016865453.1:p.Ala3860=
XM_017009965.1:c.11580C=	XP_016865454.1:p.Ala3860=
XM_017009966.2:c.11502C=	XP_016865455.1:p.Ala3834=
XM_017009967.1:c.11487C=	XP_016865456.1:p.Ala3829=
XM_017009968.2:c.11583C=	XP_016865457.1:p.Ala3861=
XM_017009969.2:c.11583C=	XP_016865458.1:p.Ala3861=
XM_017009970.2:c.11583C=	XP_016865459.1:p.Ala3861=
XM_017009971.2:c.11583C=	XP_016865460.1:p.Ala3861=
XM_017009972.1:c.4701C=	XP_016865461.1:p.Ala1567=
XM_017009973.1:c.4680C=	XP_016865462.1:p.Ala1560=
NR_003149.2:n.11578C=