Canonical Allele Identifier: CA3340104

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90694622C>T , CM000667.2:g.90694622C>T	GRCh38
NC_000005.9:g.89990439C>T , CM000667.1:g.89990439C>T	GRCh37
NC_000005.8:g.90026195C>T	NCBI36
NG_007083.1:g.140823C>T
NG_007083.2:g.170279C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.7866C>T MANE Select	NP_115495.3:p.Val2622=
ENST00000405460.9:c.7866C>T MANE Select	ENSP00000384582.2:p.Val2622=
NM_032119.3:c.7866C>T	NP_115495.3:p.Val2622=
NR_003149.1:n.7879C>T
NR_003149.2:n.7882C>T
ENST00000405460.6:c.7866C>T	ENSP00000384582.2:p.Val2622=
ENST00000509621.1:c.563C>T
ENST00000639431.1:c.265+18413C>T	ENSP00000491057.1:n.265+18413C>T
ENST00000639473.1:n.3325C>T
ENST00000640012.1:c.1673C>T
ENST00000640374.1:n.1010C>T
ENST00000640403.1:c.5157C>T	ENSP00000492531.1:p.Val1719=
ENST00000640779.1:c.2595C>T
XM_011543675.1:c.7863C>T	XP_011541977.1:p.Val2621=
XM_011543676.1:c.7785C>T	XP_011541978.1:p.Val2595=
XM_011543677.1:c.5169C>T	XP_011541979.1:p.Val1723=
XM_011543678.1:c.7866C>T	XP_011541980.1:p.Val2622=
XM_011543679.1:c.7866C>T	XP_011541981.1:p.Val2622=
XM_017009963.2:c.7866C>T	XP_016865452.1:p.Val2622=
XM_017009964.2:c.7863C>T	XP_016865453.1:p.Val2621=
XM_017009965.1:c.7863C>T	XP_016865454.1:p.Val2621=
XM_017009966.2:c.7785C>T	XP_016865455.1:p.Val2595=
XM_017009967.1:c.7770C>T	XP_016865456.1:p.Val2590=
XM_017009968.2:c.7866C>T	XP_016865457.1:p.Val2622=
XM_017009969.2:c.7866C>T	XP_016865458.1:p.Val2622=
XM_017009970.2:c.7866C>T	XP_016865459.1:p.Val2622=
XM_017009971.2:c.7866C>T	XP_016865460.1:p.Val2622=
XM_017009972.1:c.984C>T	XP_016865461.1:p.Val328=
XM_017009973.1:c.984C>T	XP_016865462.1:p.Val328=
XM_017009974.2:c.7866C>T	XP_016865463.1:p.Val2622=