Canonical Allele Identifier: CA1562918241

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823440C= , CM000667.2:g.90823440C=	GRCh38
NC_000005.9:g.90119257C= , CM000667.1:g.90119257C=	GRCh37
NC_000005.8:g.90155013C=	NCBI36
NG_007083.1:g.269641C=
NG_007083.2:g.299097C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16212C= MANE Select	ENSP00000384582.2:p.Val5404=
ENST00000425867.3:c.5166C=	ENSP00000392618.3:p.Val1722=
ENST00000638510.1:n.3479C=
ENST00000639431.1:c.265+147231C=	ENSP00000491057.1:n.265+147231C=
ENST00000640061.1:n.128+1258C=
ENST00000640407.1:c.2622C=	ENSP00000491425.1:p.Val874=
ENST00000405460.6:c.16212C=	ENSP00000384582.2:p.Val5404=
ENST00000425867.2:c.3195C=	ENSP00000392618.2:p.Val1065=
NM_032119.3:c.16212C=	NP_115495.3:p.Val5404=
NR_003149.1:n.16225C=
XM_011543675.1:c.16209C=	XP_011541977.1:p.Val5403=
XM_011543676.1:c.16131C=	XP_011541978.1:p.Val5377=
XM_011543677.1:c.13515C=	XP_011541979.1:p.Val4505=
NM_032119.4:c.16212C= MANE Select	NP_115495.3:p.Val5404=
XM_017009963.2:c.16233C=	XP_016865452.1:p.Val5411=
XM_017009964.2:c.16230C=	XP_016865453.1:p.Val5410=
XM_017009965.1:c.16230C=	XP_016865454.1:p.Val5410=
XM_017009966.2:c.16152C=	XP_016865455.1:p.Val5384=
XM_017009967.1:c.16137C=	XP_016865456.1:p.Val5379=
XM_017009968.2:c.16053C=	XP_016865457.1:p.Val5351=
XM_017009969.2:c.16233C=	XP_016865458.1:p.Val5411=
XM_017009972.1:c.9351C=	XP_016865461.1:p.Val3117=
XM_017009973.1:c.9330C=	XP_016865462.1:p.Val3110=
NR_003149.2:n.16228C=