Canonical Allele Identifier: CA445406387

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059145A>T (hg19)

Genomic Alleles

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

Transcript Alleles

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