Canonical Allele Identifier: CA1562866013

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90708822G= , CM000667.2:g.90708822G=	GRCh38
NC_000005.9:g.90004639G= , CM000667.1:g.90004639G=	GRCh37
NC_000005.8:g.90040395G=	NCBI36
NG_007083.1:g.155023G=
NG_007083.2:g.184479G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.8737G= MANE Select	ENSP00000384582.2:p.Val2913=
ENST00000639431.1:c.265+32613G=	ENSP00000491057.1:n.265+32613G=
ENST00000639473.1:n.4196G=
ENST00000640012.1:c.2544G=
ENST00000640374.1:n.1881G=
ENST00000640403.1:c.6028G=	ENSP00000492531.1:p.Val2010=
ENST00000640779.1:c.3466G=
ENST00000405460.6:c.8737G=	ENSP00000384582.2:p.Val2913=
ENST00000509621.1:c.1434G=
NM_032119.3:c.8737G=	NP_115495.3:p.Val2913=
NR_003149.1:n.8750G=
XM_011543675.1:c.8734G=	XP_011541977.1:p.Val2912=
XM_011543676.1:c.8656G=	XP_011541978.1:p.Val2886=
XM_011543677.1:c.6040G=	XP_011541979.1:p.Val2014=
XM_011543678.1:c.8737G=	XP_011541980.1:p.Val2913=
XM_011543679.1:c.8737G=	XP_011541981.1:p.Val2913=
NM_032119.4:c.8737G= MANE Select	NP_115495.3:p.Val2913=
XM_017009963.2:c.8758G=	XP_016865452.1:p.Val2920=
XM_017009964.2:c.8755G=	XP_016865453.1:p.Val2919=
XM_017009965.1:c.8755G=	XP_016865454.1:p.Val2919=
XM_017009966.2:c.8677G=	XP_016865455.1:p.Val2893=
XM_017009967.1:c.8662G=	XP_016865456.1:p.Val2888=
XM_017009968.2:c.8758G=	XP_016865457.1:p.Val2920=
XM_017009969.2:c.8758G=	XP_016865458.1:p.Val2920=
XM_017009970.2:c.8758G=	XP_016865459.1:p.Val2920=
XM_017009971.2:c.8758G=	XP_016865460.1:p.Val2920=
XM_017009972.1:c.1876G=	XP_016865461.1:p.Val626=
XM_017009973.1:c.1855G=	XP_016865462.1:p.Val619=
XM_017009974.2:c.8758G=	XP_016865463.1:p.Val2920=
NR_003149.2:n.8753G=