Canonical Allele Identifier: CA1562886251

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755213C= , CM000667.2:g.90755213C=	GRCh38
NC_000005.9:g.90051030C= , CM000667.1:g.90051030C=	GRCh37
NC_000005.8:g.90086786C=	NCBI36
NG_007083.1:g.201414C=
NG_007083.2:g.230870C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11580+28C= MANE Select	ENSP00000384582.2:n.11580+28C=
ENST00000425867.3:c.711+28C=	ENSP00000392618.3:n.711+28C=
ENST00000639431.1:c.265+79004C=	ENSP00000491057.1:n.265+79004C=
ENST00000640374.1:n.4724+28C=
ENST00000640464.1:n.1999+28C=
ENST00000405460.6:c.11580+28C=	ENSP00000384582.2:n.11580+28C=
ENST00000509621.1:c.4277+28C=
NM_032119.3:c.11580+28C=	NP_115495.3:n.11580+28C=
NR_003149.1:n.11593+28C=
XM_011543675.1:c.11577+28C=	XP_011541977.1:n.11577+28C=
XM_011543676.1:c.11499+28C=	XP_011541978.1:n.11499+28C=
XM_011543677.1:c.8883+28C=	XP_011541979.1:n.8883+28C=
XM_011543678.1:c.11580+28C=	XP_011541980.1:n.11580+28C=
NM_032119.4:c.11580+28C= MANE Select	NP_115495.3:n.11580+28C=
XM_017009963.2:c.11601+28C=	XP_016865452.1:n.11601+28C=
XM_017009964.2:c.11598+28C=	XP_016865453.1:n.11598+28C=
XM_017009965.1:c.11598+28C=	XP_016865454.1:n.11598+28C=
XM_017009966.2:c.11520+28C=	XP_016865455.1:n.11520+28C=
XM_017009967.1:c.11505+28C=	XP_016865456.1:n.11505+28C=
XM_017009968.2:c.11601+28C=	XP_016865457.1:n.11601+28C=
XM_017009969.2:c.11601+28C=	XP_016865458.1:n.11601+28C=
XM_017009970.2:c.11601+28C=	XP_016865459.1:n.11601+28C=
XM_017009971.2:c.11601+28C=	XP_016865460.1:n.11601+28C=
XM_017009972.1:c.4719+28C=	XP_016865461.1:n.4719+28C=
XM_017009973.1:c.4698+28C=	XP_016865462.1:n.4698+28C=
NR_003149.2:n.11596+28C=