Canonical Allele Identifier: CA1562901700

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789816G= , CM000667.2:g.90789816G=	GRCh38
NC_000005.9:g.90085633G= , CM000667.1:g.90085633G=	GRCh37
NC_000005.8:g.90121389G=	NCBI36
NG_007083.1:g.236017G=
NG_007083.2:g.265473G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14008G= MANE Select	ENSP00000384582.2:p.Val4670=
ENST00000425867.3:c.2962G=	ENSP00000392618.3:p.Val988=
ENST00000638510.1:n.1275G=
ENST00000638975.1:c.637G=	ENSP00000492630.1:p.Val213=
ENST00000639431.1:c.265+113607G=	ENSP00000491057.1:n.265+113607G=
ENST00000640407.1:c.418G=	ENSP00000491425.1:p.Val140=
ENST00000405460.6:c.14008G=	ENSP00000384582.2:p.Val4670=
ENST00000425867.2:c.991G=	ENSP00000392618.2:p.Val331=
NM_032119.3:c.14008G=	NP_115495.3:p.Val4670=
NR_003149.1:n.14021G=
XM_011543675.1:c.14005G=	XP_011541977.1:p.Val4669=
XM_011543676.1:c.13927G=	XP_011541978.1:p.Val4643=
XM_011543677.1:c.11311G=	XP_011541979.1:p.Val3771=
XM_011543678.1:c.14008G=	XP_011541980.1:p.Val4670=
NM_032119.4:c.14008G= MANE Select	NP_115495.3:p.Val4670=
XM_017009963.2:c.14029G=	XP_016865452.1:p.Val4677=
XM_017009964.2:c.14026G=	XP_016865453.1:p.Val4676=
XM_017009965.1:c.14026G=	XP_016865454.1:p.Val4676=
XM_017009966.2:c.13948G=	XP_016865455.1:p.Val4650=
XM_017009967.1:c.13933G=	XP_016865456.1:p.Val4645=
XM_017009968.2:c.14029G=	XP_016865457.1:p.Val4677=
XM_017009969.2:c.14029G=	XP_016865458.1:p.Val4677=
XM_017009970.2:c.14029G=	XP_016865459.1:p.Val4677=
XM_017009971.2:c.14029G=	XP_016865460.1:p.Val4677=
XM_017009972.1:c.7147G=	XP_016865461.1:p.Val2383=
XM_017009973.1:c.7126G=	XP_016865462.1:p.Val2376=
NR_003149.2:n.14024G=