Canonical Allele Identifier: CA3340350

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90708864G>A , CM000667.2:g.90708864G>A	GRCh38
NC_000005.9:g.90004681G>A , CM000667.1:g.90004681G>A	GRCh37
NC_000005.8:g.90040437G>A	NCBI36
NG_007083.1:g.155065G>A
NG_007083.2:g.184521G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8779G>A MANE Select	NP_115495.3:p.Val2927Ile
ENST00000405460.9:c.8779G>A MANE Select	ENSP00000384582.2:p.Val2927Ile
NM_032119.3:c.8779G>A	NP_115495.3:p.Val2927Ile
NR_003149.1:n.8792G>A
NR_003149.2:n.8795G>A
ENST00000405460.6:c.8779G>A	ENSP00000384582.2:p.Val2927Ile
ENST00000509621.1:c.1476G>A
ENST00000639431.1:c.265+32655G>A	ENSP00000491057.1:n.265+32655G>A
ENST00000639473.1:n.4238G>A
ENST00000640012.1:c.2586G>A
ENST00000640374.1:n.1923G>A
ENST00000640403.1:c.6070G>A	ENSP00000492531.1:p.Val2024Ile
ENST00000640779.1:c.3508G>A
XM_011543675.1:c.8776G>A	XP_011541977.1:p.Val2926Ile
XM_011543676.1:c.8698G>A	XP_011541978.1:p.Val2900Ile
XM_011543677.1:c.6082G>A	XP_011541979.1:p.Val2028Ile
XM_011543678.1:c.8779G>A	XP_011541980.1:p.Val2927Ile
XM_011543679.1:c.8779G>A	XP_011541981.1:p.Val2927Ile
XM_017009963.2:c.8800G>A	XP_016865452.1:p.Val2934Ile
XM_017009964.2:c.8797G>A	XP_016865453.1:p.Val2933Ile
XM_017009965.1:c.8797G>A	XP_016865454.1:p.Val2933Ile
XM_017009966.2:c.8719G>A	XP_016865455.1:p.Val2907Ile
XM_017009967.1:c.8704G>A	XP_016865456.1:p.Val2902Ile
XM_017009968.2:c.8800G>A	XP_016865457.1:p.Val2934Ile
XM_017009969.2:c.8800G>A	XP_016865458.1:p.Val2934Ile
XM_017009970.2:c.8800G>A	XP_016865459.1:p.Val2934Ile
XM_017009971.2:c.8800G>A	XP_016865460.1:p.Val2934Ile
XM_017009972.1:c.1918G>A	XP_016865461.1:p.Val640Ile
XM_017009973.1:c.1897G>A	XP_016865462.1:p.Val633Ile
XM_017009974.2:c.8800G>A	XP_016865463.1:p.Val2934Ile