Canonical Allele Identifier: CA3342000

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811144A>T , CM000667.2:g.90811144A>T	GRCh38
NC_000005.9:g.90106961A>T , CM000667.1:g.90106961A>T	GRCh37
NC_000005.8:g.90142717A>T	NCBI36
NG_007083.1:g.257345A>T
NG_007083.2:g.286801A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15884A>T MANE Select	NP_115495.3:p.Glu5295Val
ENST00000405460.9:c.15884A>T MANE Select	ENSP00000384582.2:p.Glu5295Val
NM_032119.3:c.15884A>T	NP_115495.3:p.Glu5295Val
NR_003149.1:n.15897A>T
NR_003149.2:n.15900A>T
ENST00000405460.6:c.15884A>T	ENSP00000384582.2:p.Glu5295Val
ENST00000425867.2:c.2867A>T	ENSP00000392618.2:p.Glu956Val
ENST00000425867.3:c.4838A>T	ENSP00000392618.3:p.Glu1613Val
ENST00000638510.1:n.3151A>T
ENST00000639431.1:c.265+134935A>T	ENSP00000491057.1:n.265+134935A>T
ENST00000640407.1:c.2294A>T	ENSP00000491425.1:p.Glu765Val
XM_011543675.1:c.15881A>T	XP_011541977.1:p.Glu5294Val
XM_011543676.1:c.15803A>T	XP_011541978.1:p.Glu5268Val
XM_011543677.1:c.13187A>T	XP_011541979.1:p.Glu4396Val
XM_017009963.2:c.15905A>T	XP_016865452.1:p.Glu5302Val
XM_017009964.2:c.15902A>T	XP_016865453.1:p.Glu5301Val
XM_017009965.1:c.15902A>T	XP_016865454.1:p.Glu5301Val
XM_017009966.2:c.15824A>T	XP_016865455.1:p.Glu5275Val
XM_017009967.1:c.15809A>T	XP_016865456.1:p.Glu5270Val
XM_017009968.2:c.15725A>T	XP_016865457.1:p.Glu5242Val
XM_017009969.2:c.15905A>T	XP_016865458.1:p.Glu5302Val
XM_017009972.1:c.9023A>T	XP_016865461.1:p.Glu3008Val
XM_017009973.1:c.9002A>T	XP_016865462.1:p.Glu3001Val