Canonical Allele Identifier: CA445466932

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979789A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90683972A>T , CM000667.2:g.90683972A>T	GRCh38
NC_000005.9:g.89979789A>T , CM000667.1:g.89979789A>T	GRCh37
NC_000005.8:g.90015545A>T	NCBI36
NG_007083.1:g.130173A>T
NG_007083.2:g.159629A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6051A>T MANE Select	ENSP00000384582.2:p.Thr2017=
ENST00000639431.1:c.265+7763A>T	ENSP00000491057.1:n.265+7763A>T
ENST00000639473.1:n.1510A>T
ENST00000640012.1:c.165-1808A>T
ENST00000640403.1:c.3342A>T	ENSP00000492531.1:p.Thr1114=
ENST00000640779.1:c.863A>T
ENST00000405460.6:c.6051A>T	ENSP00000384582.2:p.Thr2017=
NM_032119.3:c.6051A>T	NP_115495.3:p.Thr2017=
NR_003149.1:n.6147A>T
XM_011543675.1:c.6048A>T	XP_011541977.1:p.Thr2016=
XM_011543676.1:c.5970A>T	XP_011541978.1:p.Thr1990=
XM_011543677.1:c.3354A>T	XP_011541979.1:p.Thr1118=
XM_011543678.1:c.6051A>T	XP_011541980.1:p.Thr2017=
XM_011543679.1:c.6051A>T	XP_011541981.1:p.Thr2017=
NM_032119.4:c.6051A>T MANE Select	NP_115495.3:p.Thr2017=
XM_017009963.2:c.6051A>T	XP_016865452.1:p.Thr2017=
XM_017009964.2:c.6048A>T	XP_016865453.1:p.Thr2016=
XM_017009965.1:c.6048A>T	XP_016865454.1:p.Thr2016=
XM_017009966.2:c.5970A>T	XP_016865455.1:p.Thr1990=
XM_017009967.1:c.5955A>T	XP_016865456.1:p.Thr1985=
XM_017009968.2:c.6051A>T	XP_016865457.1:p.Thr2017=
XM_017009969.2:c.6051A>T	XP_016865458.1:p.Thr2017=
XM_017009970.2:c.6051A>T	XP_016865459.1:p.Thr2017=
XM_017009971.2:c.6051A>T	XP_016865460.1:p.Thr2017=
XM_017009973.1:c.-749A>T	XP_016865462.1:n.-749A>T
XM_017009974.2:c.6051A>T	XP_016865463.1:p.Thr2017=
NR_003149.2:n.6150A>T