Canonical Allele Identifier: CA1562855159

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684069G= , CM000667.2:g.90684069G=	GRCh38
NC_000005.9:g.89979886G= , CM000667.1:g.89979886G=	GRCh37
NC_000005.8:g.90015642G=	NCBI36
NG_007083.1:g.130270G=
NG_007083.2:g.159726G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6148G= MANE Select	ENSP00000384582.2:p.Gly2050=
ENST00000639431.1:c.265+7860G=	ENSP00000491057.1:n.265+7860G=
ENST00000639473.1:n.1607G=
ENST00000640012.1:c.165-1711G=
ENST00000640403.1:c.3439G=	ENSP00000492531.1:p.Gly1147=
ENST00000640779.1:c.960G=
ENST00000405460.6:c.6148G=	ENSP00000384582.2:p.Gly2050=
NM_032119.3:c.6148G=	NP_115495.3:p.Gly2050=
NR_003149.1:n.6244G=
XM_011543675.1:c.6145G=	XP_011541977.1:p.Gly2049=
XM_011543676.1:c.6067G=	XP_011541978.1:p.Gly2023=
XM_011543677.1:c.3451G=	XP_011541979.1:p.Gly1151=
XM_011543678.1:c.6148G=	XP_011541980.1:p.Gly2050=
XM_011543679.1:c.6148G=	XP_011541981.1:p.Gly2050=
NM_032119.4:c.6148G= MANE Select	NP_115495.3:p.Gly2050=
XM_017009963.2:c.6148G=	XP_016865452.1:p.Gly2050=
XM_017009964.2:c.6145G=	XP_016865453.1:p.Gly2049=
XM_017009965.1:c.6145G=	XP_016865454.1:p.Gly2049=
XM_017009966.2:c.6067G=	XP_016865455.1:p.Gly2023=
XM_017009967.1:c.6052G=	XP_016865456.1:p.Gly2018=
XM_017009968.2:c.6148G=	XP_016865457.1:p.Gly2050=
XM_017009969.2:c.6148G=	XP_016865458.1:p.Gly2050=
XM_017009970.2:c.6148G=	XP_016865459.1:p.Gly2050=
XM_017009971.2:c.6148G=	XP_016865460.1:p.Gly2050=
XM_017009973.1:c.-652G=	XP_016865462.1:n.-652G=
XM_017009974.2:c.6148G=	XP_016865463.1:p.Gly2050=
NR_003149.2:n.6247G=