Canonical Allele Identifier: CA445404614

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90692778-C-A
• MyVariant Identifiers: chr5:g.89988595C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692778C>A , CM000667.2:g.90692778C>A	GRCh38
NC_000005.9:g.89988595C>A , CM000667.1:g.89988595C>A	GRCh37
NC_000005.8:g.90024351C>A	NCBI36
NG_007083.1:g.138979C>A
NG_007083.2:g.168435C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7125C>A MANE Select	ENSP00000384582.2:p.Val2375=
ENST00000639431.1:c.265+16569C>A	ENSP00000491057.1:n.265+16569C>A
ENST00000639473.1:n.2584C>A
ENST00000640012.1:c.932C>A
ENST00000640374.1:n.269C>A
ENST00000640403.1:c.4416C>A	ENSP00000492531.1:p.Val1472=
ENST00000640779.1:c.1854C>A
ENST00000405460.6:c.7125C>A	ENSP00000384582.2:p.Val2375=
NM_032119.3:c.7125C>A	NP_115495.3:p.Val2375=
NR_003149.1:n.7138C>A
XM_011543675.1:c.7122C>A	XP_011541977.1:p.Val2374=
XM_011543676.1:c.7044C>A	XP_011541978.1:p.Val2348=
XM_011543677.1:c.4428C>A	XP_011541979.1:p.Val1476=
XM_011543678.1:c.7125C>A	XP_011541980.1:p.Val2375=
XM_011543679.1:c.7125C>A	XP_011541981.1:p.Val2375=
NM_032119.4:c.7125C>A MANE Select	NP_115495.3:p.Val2375=
XM_017009963.2:c.7125C>A	XP_016865452.1:p.Val2375=
XM_017009964.2:c.7122C>A	XP_016865453.1:p.Val2374=
XM_017009965.1:c.7122C>A	XP_016865454.1:p.Val2374=
XM_017009966.2:c.7044C>A	XP_016865455.1:p.Val2348=
XM_017009967.1:c.7029C>A	XP_016865456.1:p.Val2343=
XM_017009968.2:c.7125C>A	XP_016865457.1:p.Val2375=
XM_017009969.2:c.7125C>A	XP_016865458.1:p.Val2375=
XM_017009970.2:c.7125C>A	XP_016865459.1:p.Val2375=
XM_017009971.2:c.7125C>A	XP_016865460.1:p.Val2375=
XM_017009972.1:c.243C>A	XP_016865461.1:p.Val81=
XM_017009973.1:c.243C>A	XP_016865462.1:p.Val81=
XM_017009974.2:c.7125C>A	XP_016865463.1:p.Val2375=
NR_003149.2:n.7141C>A