Canonical Allele Identifier: CA445406770

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059217T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763400T>G , CM000667.2:g.90763400T>G	GRCh38
NC_000005.9:g.90059217T>G , CM000667.1:g.90059217T>G	GRCh37
NC_000005.8:g.90094973T>G	NCBI36
NG_007083.1:g.209601T>G
NG_007083.2:g.239057T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12216T>G MANE Select	ENSP00000384582.2:p.Leu4072=
ENST00000425867.3:c.1170T>G	ENSP00000392618.3:p.Leu390=
ENST00000639431.1:c.265+87191T>G	ENSP00000491057.1:n.265+87191T>G
ENST00000640464.1:n.2635T>G
ENST00000640729.1:n.793T>G
ENST00000405460.6:c.12216T>G	ENSP00000384582.2:p.Leu4072=
NM_032119.3:c.12216T>G	NP_115495.3:p.Leu4072=
NR_003149.1:n.12229T>G
XM_011543675.1:c.12213T>G	XP_011541977.1:p.Leu4071=
XM_011543676.1:c.12135T>G	XP_011541978.1:p.Leu4045=
XM_011543677.1:c.9519T>G	XP_011541979.1:p.Leu3173=
XM_011543678.1:c.12216T>G	XP_011541980.1:p.Leu4072=
NM_032119.4:c.12216T>G MANE Select	NP_115495.3:p.Leu4072=
XM_017009963.2:c.12237T>G	XP_016865452.1:p.Leu4079=
XM_017009964.2:c.12234T>G	XP_016865453.1:p.Leu4078=
XM_017009965.1:c.12234T>G	XP_016865454.1:p.Leu4078=
XM_017009966.2:c.12156T>G	XP_016865455.1:p.Leu4052=
XM_017009967.1:c.12141T>G	XP_016865456.1:p.Leu4047=
XM_017009968.2:c.12237T>G	XP_016865457.1:p.Leu4079=
XM_017009969.2:c.12237T>G	XP_016865458.1:p.Leu4079=
XM_017009970.2:c.12237T>G	XP_016865459.1:p.Leu4079=
XM_017009971.2:c.12237T>G	XP_016865460.1:p.Leu4079=
XM_017009972.1:c.5355T>G	XP_016865461.1:p.Leu1785=
XM_017009973.1:c.5334T>G	XP_016865462.1:p.Leu1778=
NR_003149.2:n.12232T>G