Canonical Allele Identifier: CA1562889875

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763341G= , CM000667.2:g.90763341G=	GRCh38
NC_000005.9:g.90059158G= , CM000667.1:g.90059158G=	GRCh37
NC_000005.8:g.90094914G=	NCBI36
NG_007083.1:g.209542G=
NG_007083.2:g.238998G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12157G= MANE Select	ENSP00000384582.2:p.Asp4053=
ENST00000425867.3:c.1111G=	ENSP00000392618.3:p.Asp371=
ENST00000639431.1:c.265+87132G=	ENSP00000491057.1:n.265+87132G=
ENST00000640464.1:n.2576G=
ENST00000640729.1:n.734G=
ENST00000405460.6:c.12157G=	ENSP00000384582.2:p.Asp4053=
NM_032119.3:c.12157G=	NP_115495.3:p.Asp4053=
NR_003149.1:n.12170G=
XM_011543675.1:c.12154G=	XP_011541977.1:p.Asp4052=
XM_011543676.1:c.12076G=	XP_011541978.1:p.Asp4026=
XM_011543677.1:c.9460G=	XP_011541979.1:p.Asp3154=
XM_011543678.1:c.12157G=	XP_011541980.1:p.Asp4053=
NM_032119.4:c.12157G= MANE Select	NP_115495.3:p.Asp4053=
XM_017009963.2:c.12178G=	XP_016865452.1:p.Asp4060=
XM_017009964.2:c.12175G=	XP_016865453.1:p.Asp4059=
XM_017009965.1:c.12175G=	XP_016865454.1:p.Asp4059=
XM_017009966.2:c.12097G=	XP_016865455.1:p.Asp4033=
XM_017009967.1:c.12082G=	XP_016865456.1:p.Asp4028=
XM_017009968.2:c.12178G=	XP_016865457.1:p.Asp4060=
XM_017009969.2:c.12178G=	XP_016865458.1:p.Asp4060=
XM_017009970.2:c.12178G=	XP_016865459.1:p.Asp4060=
XM_017009971.2:c.12178G=	XP_016865460.1:p.Asp4060=
XM_017009972.1:c.5296G=	XP_016865461.1:p.Asp1766=
XM_017009973.1:c.5275G=	XP_016865462.1:p.Asp1759=
NR_003149.2:n.12173G=