Canonical Allele Identifier: CA1562825200

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90618220C= , CM000667.2:g.90618220C=	GRCh38
NC_000005.9:g.89914037C= , CM000667.1:g.89914037C=	GRCh37
NC_000005.8:g.89949793C=	NCBI36
NG_007083.1:g.64421C=
NG_007083.2:g.93877C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.357+267C= MANE Select	ENSP00000384582.2:n.357+267C=
ENST00000638316.1:n.567+267C=
ENST00000638638.1:n.764+267C=
ENST00000640083.1:n.62+267C=
ENST00000640109.1:n.453+267C=
ENST00000640281.1:n.416+267C=
ENST00000405460.6:c.357+267C=	ENSP00000384582.2:n.357+267C=
ENST00000508842.5:c.369+267C=	ENSP00000425936.1:n.369+267C=
NM_032119.3:c.357+267C=	NP_115495.3:n.357+267C=
NR_003149.1:n.453+267C=
XM_011543675.1:c.357+267C=	XP_011541977.1:n.357+267C=
XM_011543676.1:c.357+267C=	XP_011541978.1:n.357+267C=
XM_011543678.1:c.357+267C=	XP_011541980.1:n.357+267C=
XM_011543679.1:c.357+267C=	XP_011541981.1:n.357+267C=
NM_032119.4:c.357+267C= MANE Select	NP_115495.3:n.357+267C=
XM_017009963.2:c.357+267C=	XP_016865452.1:n.357+267C=
XM_017009964.2:c.357+267C=	XP_016865453.1:n.357+267C=
XM_017009965.1:c.354+267C=	XP_016865454.1:n.354+267C=
XM_017009966.2:c.357+267C=	XP_016865455.1:n.357+267C=
XM_017009967.1:c.357+267C=	XP_016865456.1:n.357+267C=
XM_017009968.2:c.357+267C=	XP_016865457.1:n.357+267C=
XM_017009969.2:c.357+267C=	XP_016865458.1:n.357+267C=
XM_017009970.2:c.357+267C=	XP_016865459.1:n.357+267C=
XM_017009971.2:c.357+267C=	XP_016865460.1:n.357+267C=
XM_017009974.2:c.357+267C=	XP_016865463.1:n.357+267C=
NR_003149.2:n.456+267C=