Canonical Allele Identifier: CA1562882072

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745622A= , CM000667.2:g.90745622A=	GRCh38
NC_000005.9:g.90041439A= , CM000667.1:g.90041439A=	GRCh37
NC_000005.8:g.90077195A=	NCBI36
NG_007083.1:g.191823A=
NG_007083.2:g.221279A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10801A= MANE Select	ENSP00000384582.2:p.Arg3601=
ENST00000639431.1:c.265+69413A=	ENSP00000491057.1:n.265+69413A=
ENST00000640374.1:n.3945A=
ENST00000640464.1:n.1220A=
ENST00000405460.6:c.10801A=	ENSP00000384582.2:p.Arg3601=
ENST00000509621.1:c.3498A=
NM_032119.3:c.10801A=	NP_115495.3:p.Arg3601=
NR_003149.1:n.10814A=
XM_011543675.1:c.10798A=	XP_011541977.1:p.Arg3600=
XM_011543676.1:c.10720A=	XP_011541978.1:p.Arg3574=
XM_011543677.1:c.8104A=	XP_011541979.1:p.Arg2702=
XM_011543678.1:c.10801A=	XP_011541980.1:p.Arg3601=
XM_011543679.1:c.*23A=	XP_011541981.1:n.*23A=
NM_032119.4:c.10801A= MANE Select	NP_115495.3:p.Arg3601=
XM_017009963.2:c.10822A=	XP_016865452.1:p.Arg3608=
XM_017009964.2:c.10819A=	XP_016865453.1:p.Arg3607=
XM_017009965.1:c.10819A=	XP_016865454.1:p.Arg3607=
XM_017009966.2:c.10741A=	XP_016865455.1:p.Arg3581=
XM_017009967.1:c.10726A=	XP_016865456.1:p.Arg3576=
XM_017009968.2:c.10822A=	XP_016865457.1:p.Arg3608=
XM_017009969.2:c.10822A=	XP_016865458.1:p.Arg3608=
XM_017009970.2:c.10822A=	XP_016865459.1:p.Arg3608=
XM_017009971.2:c.10822A=	XP_016865460.1:p.Arg3608=
XM_017009972.1:c.3940A=	XP_016865461.1:p.Arg1314=
XM_017009973.1:c.3919A=	XP_016865462.1:p.Arg1307=
XM_017009974.2:c.*23A=	XP_016865463.1:n.*23A=
NR_003149.2:n.10817A=