Canonical Allele Identifier: CA445404095

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050900C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755083C>G , CM000667.2:g.90755083C>G	GRCh38
NC_000005.9:g.90050900C>G , CM000667.1:g.90050900C>G	GRCh37
NC_000005.8:g.90086656C>G	NCBI36
NG_007083.1:g.201284C>G
NG_007083.2:g.230740C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11478C>G MANE Select	ENSP00000384582.2:p.Val3826=
ENST00000425867.3:c.609C>G	ENSP00000392618.3:p.Val203=
ENST00000639431.1:c.265+78874C>G	ENSP00000491057.1:n.265+78874C>G
ENST00000640374.1:n.4622C>G
ENST00000640464.1:n.1897C>G
ENST00000405460.6:c.11478C>G	ENSP00000384582.2:p.Val3826=
ENST00000509621.1:c.4175C>G
NM_032119.3:c.11478C>G	NP_115495.3:p.Val3826=
NR_003149.1:n.11491C>G
XM_011543675.1:c.11475C>G	XP_011541977.1:p.Val3825=
XM_011543676.1:c.11397C>G	XP_011541978.1:p.Val3799=
XM_011543677.1:c.8781C>G	XP_011541979.1:p.Val2927=
XM_011543678.1:c.11478C>G	XP_011541980.1:p.Val3826=
NM_032119.4:c.11478C>G MANE Select	NP_115495.3:p.Val3826=
XM_017009963.2:c.11499C>G	XP_016865452.1:p.Val3833=
XM_017009964.2:c.11496C>G	XP_016865453.1:p.Val3832=
XM_017009965.1:c.11496C>G	XP_016865454.1:p.Val3832=
XM_017009966.2:c.11418C>G	XP_016865455.1:p.Val3806=
XM_017009967.1:c.11403C>G	XP_016865456.1:p.Val3801=
XM_017009968.2:c.11499C>G	XP_016865457.1:p.Val3833=
XM_017009969.2:c.11499C>G	XP_016865458.1:p.Val3833=
XM_017009970.2:c.11499C>G	XP_016865459.1:p.Val3833=
XM_017009971.2:c.11499C>G	XP_016865460.1:p.Val3833=
XM_017009972.1:c.4617C>G	XP_016865461.1:p.Val1539=
XM_017009973.1:c.4596C>G	XP_016865462.1:p.Val1532=
NR_003149.2:n.11494C>G