Canonical Allele Identifier: CA445406393

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90763331-C-A
• MyVariant Identifiers: chr5:g.90059148C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763331C>A , CM000667.2:g.90763331C>A	GRCh38
NC_000005.9:g.90059148C>A , CM000667.1:g.90059148C>A	GRCh37
NC_000005.8:g.90094904C>A	NCBI36
NG_007083.1:g.209532C>A
NG_007083.2:g.238988C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12147C>A MANE Select	ENSP00000384582.2:p.Ser4049=
ENST00000425867.3:c.1101C>A	ENSP00000392618.3:p.Ser367=
ENST00000639431.1:c.265+87122C>A	ENSP00000491057.1:n.265+87122C>A
ENST00000640464.1:n.2566C>A
ENST00000640729.1:n.724C>A
ENST00000405460.6:c.12147C>A	ENSP00000384582.2:p.Ser4049=
NM_032119.3:c.12147C>A	NP_115495.3:p.Ser4049=
NR_003149.1:n.12160C>A
XM_011543675.1:c.12144C>A	XP_011541977.1:p.Ser4048=
XM_011543676.1:c.12066C>A	XP_011541978.1:p.Ser4022=
XM_011543677.1:c.9450C>A	XP_011541979.1:p.Ser3150=
XM_011543678.1:c.12147C>A	XP_011541980.1:p.Ser4049=
NM_032119.4:c.12147C>A MANE Select	NP_115495.3:p.Ser4049=
XM_017009963.2:c.12168C>A	XP_016865452.1:p.Ser4056=
XM_017009964.2:c.12165C>A	XP_016865453.1:p.Ser4055=
XM_017009965.1:c.12165C>A	XP_016865454.1:p.Ser4055=
XM_017009966.2:c.12087C>A	XP_016865455.1:p.Ser4029=
XM_017009967.1:c.12072C>A	XP_016865456.1:p.Ser4024=
XM_017009968.2:c.12168C>A	XP_016865457.1:p.Ser4056=
XM_017009969.2:c.12168C>A	XP_016865458.1:p.Ser4056=
XM_017009970.2:c.12168C>A	XP_016865459.1:p.Ser4056=
XM_017009971.2:c.12168C>A	XP_016865460.1:p.Ser4056=
XM_017009972.1:c.5286C>A	XP_016865461.1:p.Ser1762=
XM_017009973.1:c.5265C>A	XP_016865462.1:p.Ser1755=
NR_003149.2:n.12163C>A