Canonical Allele Identifier: CA445406386

Gene: ADGRV1

Linked Data

• dbSNP Id: rs2150014866
• MyVariant Identifiers: chr5:g.90059145A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763328A>G , CM000667.2:g.90763328A>G	GRCh38
NC_000005.9:g.90059145A>G , CM000667.1:g.90059145A>G	GRCh37
NC_000005.8:g.90094901A>G	NCBI36
NG_007083.1:g.209529A>G
NG_007083.2:g.238985A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12144A>G MANE Select	ENSP00000384582.2:p.Ser4048=
ENST00000425867.3:c.1098A>G	ENSP00000392618.3:p.Ser366=
ENST00000639431.1:c.265+87119A>G	ENSP00000491057.1:n.265+87119A>G
ENST00000640464.1:n.2563A>G
ENST00000640729.1:n.721A>G
ENST00000405460.6:c.12144A>G	ENSP00000384582.2:p.Ser4048=
NM_032119.3:c.12144A>G	NP_115495.3:p.Ser4048=
NR_003149.1:n.12157A>G
XM_011543675.1:c.12141A>G	XP_011541977.1:p.Ser4047=
XM_011543676.1:c.12063A>G	XP_011541978.1:p.Ser4021=
XM_011543677.1:c.9447A>G	XP_011541979.1:p.Ser3149=
XM_011543678.1:c.12144A>G	XP_011541980.1:p.Ser4048=
NM_032119.4:c.12144A>G MANE Select	NP_115495.3:p.Ser4048=
XM_017009963.2:c.12165A>G	XP_016865452.1:p.Ser4055=
XM_017009964.2:c.12162A>G	XP_016865453.1:p.Ser4054=
XM_017009965.1:c.12162A>G	XP_016865454.1:p.Ser4054=
XM_017009966.2:c.12084A>G	XP_016865455.1:p.Ser4028=
XM_017009967.1:c.12069A>G	XP_016865456.1:p.Ser4023=
XM_017009968.2:c.12165A>G	XP_016865457.1:p.Ser4055=
XM_017009969.2:c.12165A>G	XP_016865458.1:p.Ser4055=
XM_017009970.2:c.12165A>G	XP_016865459.1:p.Ser4055=
XM_017009971.2:c.12165A>G	XP_016865460.1:p.Ser4055=
XM_017009972.1:c.5283A>G	XP_016865461.1:p.Ser1761=
XM_017009973.1:c.5262A>G	XP_016865462.1:p.Ser1754=
NR_003149.2:n.12160A>G