Canonical Allele Identifier: CA1562886219

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755128A= , CM000667.2:g.90755128A=	GRCh38
NC_000005.9:g.90050945A= , CM000667.1:g.90050945A=	GRCh37
NC_000005.8:g.90086701A=	NCBI36
NG_007083.1:g.201329A=
NG_007083.2:g.230785A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11523A= MANE Select	ENSP00000384582.2:p.Thr3841=
ENST00000425867.3:c.654A=	ENSP00000392618.3:p.Thr218=
ENST00000639431.1:c.265+78919A=	ENSP00000491057.1:n.265+78919A=
ENST00000640374.1:n.4667A=
ENST00000640464.1:n.1942A=
ENST00000405460.6:c.11523A=	ENSP00000384582.2:p.Thr3841=
ENST00000509621.1:c.4220A=
NM_032119.3:c.11523A=	NP_115495.3:p.Thr3841=
NR_003149.1:n.11536A=
XM_011543675.1:c.11520A=	XP_011541977.1:p.Thr3840=
XM_011543676.1:c.11442A=	XP_011541978.1:p.Thr3814=
XM_011543677.1:c.8826A=	XP_011541979.1:p.Thr2942=
XM_011543678.1:c.11523A=	XP_011541980.1:p.Thr3841=
NM_032119.4:c.11523A= MANE Select	NP_115495.3:p.Thr3841=
XM_017009963.2:c.11544A=	XP_016865452.1:p.Thr3848=
XM_017009964.2:c.11541A=	XP_016865453.1:p.Thr3847=
XM_017009965.1:c.11541A=	XP_016865454.1:p.Thr3847=
XM_017009966.2:c.11463A=	XP_016865455.1:p.Thr3821=
XM_017009967.1:c.11448A=	XP_016865456.1:p.Thr3816=
XM_017009968.2:c.11544A=	XP_016865457.1:p.Thr3848=
XM_017009969.2:c.11544A=	XP_016865458.1:p.Thr3848=
XM_017009970.2:c.11544A=	XP_016865459.1:p.Thr3848=
XM_017009971.2:c.11544A=	XP_016865460.1:p.Thr3848=
XM_017009972.1:c.4662A=	XP_016865461.1:p.Thr1554=
XM_017009973.1:c.4641A=	XP_016865462.1:p.Thr1547=
NR_003149.2:n.11539A=