Canonical Allele Identifier: CA1562882112

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745719A= , CM000667.2:g.90745719A=	GRCh38
NC_000005.9:g.90041536A= , CM000667.1:g.90041536A=	GRCh37
NC_000005.8:g.90077292A=	NCBI36
NG_007083.1:g.191920A=
NG_007083.2:g.221376A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10898A= MANE Select	ENSP00000384582.2:p.Glu3633=
ENST00000425867.3:c.29A=	ENSP00000392618.3:p.Glu10=
ENST00000639431.1:c.265+69510A=	ENSP00000491057.1:n.265+69510A=
ENST00000640374.1:n.4042A=
ENST00000640464.1:n.1317A=
ENST00000405460.6:c.10898A=	ENSP00000384582.2:p.Glu3633=
ENST00000509621.1:c.3595A=
NM_032119.3:c.10898A=	NP_115495.3:p.Glu3633=
NR_003149.1:n.10911A=
XM_011543675.1:c.10895A=	XP_011541977.1:p.Glu3632=
XM_011543676.1:c.10817A=	XP_011541978.1:p.Glu3606=
XM_011543677.1:c.8201A=	XP_011541979.1:p.Glu2734=
XM_011543678.1:c.10898A=	XP_011541980.1:p.Glu3633=
NM_032119.4:c.10898A= MANE Select	NP_115495.3:p.Glu3633=
XM_017009963.2:c.10919A=	XP_016865452.1:p.Glu3640=
XM_017009964.2:c.10916A=	XP_016865453.1:p.Glu3639=
XM_017009965.1:c.10916A=	XP_016865454.1:p.Glu3639=
XM_017009966.2:c.10838A=	XP_016865455.1:p.Glu3613=
XM_017009967.1:c.10823A=	XP_016865456.1:p.Glu3608=
XM_017009968.2:c.10919A=	XP_016865457.1:p.Glu3640=
XM_017009969.2:c.10919A=	XP_016865458.1:p.Glu3640=
XM_017009970.2:c.10919A=	XP_016865459.1:p.Glu3640=
XM_017009971.2:c.10919A=	XP_016865460.1:p.Glu3640=
XM_017009972.1:c.4037A=	XP_016865461.1:p.Glu1346=
XM_017009973.1:c.4016A=	XP_016865462.1:p.Glu1339=
NR_003149.2:n.10914A=