Canonical Allele Identifier: CA445404183

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050963A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755146A>G , CM000667.2:g.90755146A>G	GRCh38
NC_000005.9:g.90050963A>G , CM000667.1:g.90050963A>G	GRCh37
NC_000005.8:g.90086719A>G	NCBI36
NG_007083.1:g.201347A>G
NG_007083.2:g.230803A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11541A>G MANE Select	ENSP00000384582.2:p.Glu3847=
ENST00000425867.3:c.672A>G	ENSP00000392618.3:p.Glu224=
ENST00000639431.1:c.265+78937A>G	ENSP00000491057.1:n.265+78937A>G
ENST00000640374.1:n.4685A>G
ENST00000640464.1:n.1960A>G
ENST00000405460.6:c.11541A>G	ENSP00000384582.2:p.Glu3847=
ENST00000509621.1:c.4238A>G
NM_032119.3:c.11541A>G	NP_115495.3:p.Glu3847=
NR_003149.1:n.11554A>G
XM_011543675.1:c.11538A>G	XP_011541977.1:p.Glu3846=
XM_011543676.1:c.11460A>G	XP_011541978.1:p.Glu3820=
XM_011543677.1:c.8844A>G	XP_011541979.1:p.Glu2948=
XM_011543678.1:c.11541A>G	XP_011541980.1:p.Glu3847=
NM_032119.4:c.11541A>G MANE Select	NP_115495.3:p.Glu3847=
XM_017009963.2:c.11562A>G	XP_016865452.1:p.Glu3854=
XM_017009964.2:c.11559A>G	XP_016865453.1:p.Glu3853=
XM_017009965.1:c.11559A>G	XP_016865454.1:p.Glu3853=
XM_017009966.2:c.11481A>G	XP_016865455.1:p.Glu3827=
XM_017009967.1:c.11466A>G	XP_016865456.1:p.Glu3822=
XM_017009968.2:c.11562A>G	XP_016865457.1:p.Glu3854=
XM_017009969.2:c.11562A>G	XP_016865458.1:p.Glu3854=
XM_017009970.2:c.11562A>G	XP_016865459.1:p.Glu3854=
XM_017009971.2:c.11562A>G	XP_016865460.1:p.Glu3854=
XM_017009972.1:c.4680A>G	XP_016865461.1:p.Glu1560=
XM_017009973.1:c.4659A>G	XP_016865462.1:p.Glu1553=
NR_003149.2:n.11557A>G