Canonical Allele Identifier: CA360425468

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1470053497
• MyVariant Identifiers: chr5:g.90119255G>A (hg19) ; chr5:g.90823438G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823438G>A , CM000667.2:g.90823438G>A	GRCh38
NC_000005.9:g.90119255G>A , CM000667.1:g.90119255G>A	GRCh37
NC_000005.8:g.90155011G>A	NCBI36
NG_007083.1:g.269639G>A
NG_007083.2:g.299095G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16210G>A MANE Select	ENSP00000384582.2:p.Val5404Ile
ENST00000425867.3:c.5164G>A	ENSP00000392618.3:p.Val1722Ile
ENST00000638510.1:n.3477G>A
ENST00000639431.1:c.265+147229G>A	ENSP00000491057.1:n.265+147229G>A
ENST00000640061.1:n.128+1256G>A
ENST00000640407.1:c.2620G>A	ENSP00000491425.1:p.Val874Ile
ENST00000405460.6:c.16210G>A	ENSP00000384582.2:p.Val5404Ile
ENST00000425867.2:c.3193G>A	ENSP00000392618.2:p.Val1065Ile
NM_032119.3:c.16210G>A	NP_115495.3:p.Val5404Ile
NR_003149.1:n.16223G>A
XM_011543675.1:c.16207G>A	XP_011541977.1:p.Val5403Ile
XM_011543676.1:c.16129G>A	XP_011541978.1:p.Val5377Ile
XM_011543677.1:c.13513G>A	XP_011541979.1:p.Val4505Ile
NM_032119.4:c.16210G>A MANE Select	NP_115495.3:p.Val5404Ile
XM_017009963.2:c.16231G>A	XP_016865452.1:p.Val5411Ile
XM_017009964.2:c.16228G>A	XP_016865453.1:p.Val5410Ile
XM_017009965.1:c.16228G>A	XP_016865454.1:p.Val5410Ile
XM_017009966.2:c.16150G>A	XP_016865455.1:p.Val5384Ile
XM_017009967.1:c.16135G>A	XP_016865456.1:p.Val5379Ile
XM_017009968.2:c.16051G>A	XP_016865457.1:p.Val5351Ile
XM_017009969.2:c.16231G>A	XP_016865458.1:p.Val5411Ile
XM_017009972.1:c.9349G>A	XP_016865461.1:p.Val3117Ile
XM_017009973.1:c.9328G>A	XP_016865462.1:p.Val3110Ile
NR_003149.2:n.16226G>A