Canonical Allele Identifier: CA445416125

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041504A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745687A>G , CM000667.2:g.90745687A>G	GRCh38
NC_000005.9:g.90041504A>G , CM000667.1:g.90041504A>G	GRCh37
NC_000005.8:g.90077260A>G	NCBI36
NG_007083.1:g.191888A>G
NG_007083.2:g.221344A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10866A>G MANE Select	ENSP00000384582.2:p.Lys3622=
ENST00000639431.1:c.265+69478A>G	ENSP00000491057.1:n.265+69478A>G
ENST00000640374.1:n.4010A>G
ENST00000640464.1:n.1285A>G
ENST00000405460.6:c.10866A>G	ENSP00000384582.2:p.Lys3622=
ENST00000509621.1:c.3563A>G
NM_032119.3:c.10866A>G	NP_115495.3:p.Lys3622=
NR_003149.1:n.10879A>G
XM_011543675.1:c.10863A>G	XP_011541977.1:p.Lys3621=
XM_011543676.1:c.10785A>G	XP_011541978.1:p.Lys3595=
XM_011543677.1:c.8169A>G	XP_011541979.1:p.Lys2723=
XM_011543678.1:c.10866A>G	XP_011541980.1:p.Lys3622=
NM_032119.4:c.10866A>G MANE Select	NP_115495.3:p.Lys3622=
XM_017009963.2:c.10887A>G	XP_016865452.1:p.Lys3629=
XM_017009964.2:c.10884A>G	XP_016865453.1:p.Lys3628=
XM_017009965.1:c.10884A>G	XP_016865454.1:p.Lys3628=
XM_017009966.2:c.10806A>G	XP_016865455.1:p.Lys3602=
XM_017009967.1:c.10791A>G	XP_016865456.1:p.Lys3597=
XM_017009968.2:c.10887A>G	XP_016865457.1:p.Lys3629=
XM_017009969.2:c.10887A>G	XP_016865458.1:p.Lys3629=
XM_017009970.2:c.10887A>G	XP_016865459.1:p.Lys3629=
XM_017009971.2:c.10887A>G	XP_016865460.1:p.Lys3629=
XM_017009972.1:c.4005A>G	XP_016865461.1:p.Lys1335=
XM_017009973.1:c.3984A>G	XP_016865462.1:p.Lys1328=
NR_003149.2:n.10882A>G