Canonical Allele Identifier: CA445416146

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1754548709
• gnomAD v4: 5-90745705-C-A
• MyVariant Identifiers: chr5:g.90041522C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745705C>A , CM000667.2:g.90745705C>A	GRCh38
NC_000005.9:g.90041522C>A , CM000667.1:g.90041522C>A	GRCh37
NC_000005.8:g.90077278C>A	NCBI36
NG_007083.1:g.191906C>A
NG_007083.2:g.221362C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10884C>A MANE Select	ENSP00000384582.2:p.Pro3628=
ENST00000425867.3:c.15C>A	ENSP00000392618.3:p.Pro5=
ENST00000639431.1:c.265+69496C>A	ENSP00000491057.1:n.265+69496C>A
ENST00000640374.1:n.4028C>A
ENST00000640464.1:n.1303C>A
ENST00000405460.6:c.10884C>A	ENSP00000384582.2:p.Pro3628=
ENST00000509621.1:c.3581C>A
NM_032119.3:c.10884C>A	NP_115495.3:p.Pro3628=
NR_003149.1:n.10897C>A
XM_011543675.1:c.10881C>A	XP_011541977.1:p.Pro3627=
XM_011543676.1:c.10803C>A	XP_011541978.1:p.Pro3601=
XM_011543677.1:c.8187C>A	XP_011541979.1:p.Pro2729=
XM_011543678.1:c.10884C>A	XP_011541980.1:p.Pro3628=
NM_032119.4:c.10884C>A MANE Select	NP_115495.3:p.Pro3628=
XM_017009963.2:c.10905C>A	XP_016865452.1:p.Pro3635=
XM_017009964.2:c.10902C>A	XP_016865453.1:p.Pro3634=
XM_017009965.1:c.10902C>A	XP_016865454.1:p.Pro3634=
XM_017009966.2:c.10824C>A	XP_016865455.1:p.Pro3608=
XM_017009967.1:c.10809C>A	XP_016865456.1:p.Pro3603=
XM_017009968.2:c.10905C>A	XP_016865457.1:p.Pro3635=
XM_017009969.2:c.10905C>A	XP_016865458.1:p.Pro3635=
XM_017009970.2:c.10905C>A	XP_016865459.1:p.Pro3635=
XM_017009971.2:c.10905C>A	XP_016865460.1:p.Pro3635=
XM_017009972.1:c.4023C>A	XP_016865461.1:p.Pro1341=
XM_017009973.1:c.4002C>A	XP_016865462.1:p.Pro1334=
NR_003149.2:n.10900C>A