Canonical Allele Identifier: CA1562875039

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90729080G= , CM000667.2:g.90729080G=	GRCh38
NC_000005.9:g.90024897G= , CM000667.1:g.90024897G=	GRCh37
NC_000005.8:g.90060653G=	NCBI36
NG_007083.1:g.175281G=
NG_007083.2:g.204737G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10426+147G= MANE Select	ENSP00000384582.2:n.10426+147G=
ENST00000639431.1:c.265+52871G=	ENSP00000491057.1:n.265+52871G=
ENST00000640374.1:n.3570+147G=
ENST00000640464.1:n.845+147G=
ENST00000405460.6:c.10426+147G=	ENSP00000384582.2:n.10426+147G=
ENST00000509621.1:c.3123+147G=
NM_032119.3:c.10426+147G=	NP_115495.3:n.10426+147G=
NR_003149.1:n.10439+147G=
XM_011543675.1:c.10423+147G=	XP_011541977.1:n.10423+147G=
XM_011543676.1:c.10345+147G=	XP_011541978.1:n.10345+147G=
XM_011543677.1:c.7729+147G=	XP_011541979.1:n.7729+147G=
XM_011543678.1:c.10426+147G=	XP_011541980.1:n.10426+147G=
XM_011543679.1:c.10426+147G=	XP_011541981.1:n.10426+147G=
XR_948560.1:n.271+11827C=
NM_032119.4:c.10426+147G= MANE Select	NP_115495.3:n.10426+147G=
XM_017009963.2:c.10447+147G=	XP_016865452.1:n.10447+147G=
XM_017009964.2:c.10444+147G=	XP_016865453.1:n.10444+147G=
XM_017009965.1:c.10444+147G=	XP_016865454.1:n.10444+147G=
XM_017009966.2:c.10366+147G=	XP_016865455.1:n.10366+147G=
XM_017009967.1:c.10351+147G=	XP_016865456.1:n.10351+147G=
XM_017009968.2:c.10447+147G=	XP_016865457.1:n.10447+147G=
XM_017009969.2:c.10447+147G=	XP_016865458.1:n.10447+147G=
XM_017009970.2:c.10447+147G=	XP_016865459.1:n.10447+147G=
XM_017009971.2:c.10447+147G=	XP_016865460.1:n.10447+147G=
XM_017009972.1:c.3565+147G=	XP_016865461.1:n.3565+147G=
XM_017009973.1:c.3544+147G=	XP_016865462.1:n.3544+147G=
XM_017009974.2:c.10447+147G=	XP_016865463.1:n.10447+147G=
XR_001742802.1:n.2522+11827C=
NR_003149.2:n.10442+147G=