Canonical Allele Identifier: CA1562901685

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789778C= , CM000667.2:g.90789778C=	GRCh38
NC_000005.9:g.90085595C= , CM000667.1:g.90085595C=	GRCh37
NC_000005.8:g.90121351C=	NCBI36
NG_007083.1:g.235979C=
NG_007083.2:g.265435C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.13970C= MANE Select	ENSP00000384582.2:p.Pro4657=
ENST00000425867.3:c.2924C=	ENSP00000392618.3:p.Pro975=
ENST00000638510.1:n.1237C=
ENST00000638975.1:c.599C=	ENSP00000492630.1:p.Pro200=
ENST00000639431.1:c.265+113569C=	ENSP00000491057.1:n.265+113569C=
ENST00000640407.1:c.380C=	ENSP00000491425.1:p.Pro127=
ENST00000405460.6:c.13970C=	ENSP00000384582.2:p.Pro4657=
ENST00000425867.2:c.953C=	ENSP00000392618.2:p.Pro318=
NM_032119.3:c.13970C=	NP_115495.3:p.Pro4657=
NR_003149.1:n.13983C=
XM_011543675.1:c.13967C=	XP_011541977.1:p.Pro4656=
XM_011543676.1:c.13889C=	XP_011541978.1:p.Pro4630=
XM_011543677.1:c.11273C=	XP_011541979.1:p.Pro3758=
XM_011543678.1:c.13970C=	XP_011541980.1:p.Pro4657=
NM_032119.4:c.13970C= MANE Select	NP_115495.3:p.Pro4657=
XM_017009963.2:c.13991C=	XP_016865452.1:p.Pro4664=
XM_017009964.2:c.13988C=	XP_016865453.1:p.Pro4663=
XM_017009965.1:c.13988C=	XP_016865454.1:p.Pro4663=
XM_017009966.2:c.13910C=	XP_016865455.1:p.Pro4637=
XM_017009967.1:c.13895C=	XP_016865456.1:p.Pro4632=
XM_017009968.2:c.13991C=	XP_016865457.1:p.Pro4664=
XM_017009969.2:c.13991C=	XP_016865458.1:p.Pro4664=
XM_017009970.2:c.13991C=	XP_016865459.1:p.Pro4664=
XM_017009971.2:c.13991C=	XP_016865460.1:p.Pro4664=
XM_017009972.1:c.7109C=	XP_016865461.1:p.Pro2370=
XM_017009973.1:c.7088C=	XP_016865462.1:p.Pro2363=
NR_003149.2:n.13986C=