Canonical Allele Identifier: CA3338427

Gene: ADGRV1

Linked Data

• ClinVar Variation Id: 965477
• ClinVar RCV Id: RCV001239935
• dbSNP Id: rs533094348
• ExAC: 5:89913681 G / A
• gnomAD v2: 5-89913681-G-A
• gnomAD v3: 5-90617864-G-A
• gnomAD v4: 5-90617864-G-A
• MyVariant Identifiers: chr5:g.89913681G>A (hg19) ; chr5:g.90617864G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617864G>A , CM000667.2:g.90617864G>A	GRCh38
NC_000005.9:g.89913681G>A , CM000667.1:g.89913681G>A	GRCh37
NC_000005.8:g.89949437G>A	NCBI36
NG_007083.1:g.64065G>A
NG_007083.2:g.93521G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.268G>A MANE Select	ENSP00000384582.2:p.Gly90Arg
ENST00000638316.1:n.478G>A
ENST00000638638.1:n.675G>A
ENST00000640109.1:n.364G>A
ENST00000640281.1:n.327G>A
ENST00000405460.6:c.268G>A	ENSP00000384582.2:p.Gly90Arg
ENST00000508842.5:c.280G>A	ENSP00000425936.1:p.Gly94Arg
NM_032119.3:c.268G>A	NP_115495.3:p.Gly90Arg
NR_003149.1:n.364G>A
XM_011543675.1:c.268G>A	XP_011541977.1:p.Gly90Arg
XM_011543676.1:c.268G>A	XP_011541978.1:p.Gly90Arg
XM_011543678.1:c.268G>A	XP_011541980.1:p.Gly90Arg
XM_011543679.1:c.268G>A	XP_011541981.1:p.Gly90Arg
NM_032119.4:c.268G>A MANE Select	NP_115495.3:p.Gly90Arg
XM_017009963.2:c.268G>A	XP_016865452.1:p.Gly90Arg
XM_017009964.2:c.268G>A	XP_016865453.1:p.Gly90Arg
XM_017009965.1:c.265G>A	XP_016865454.1:p.Gly89Arg
XM_017009966.2:c.268G>A	XP_016865455.1:p.Gly90Arg
XM_017009967.1:c.268G>A	XP_016865456.1:p.Gly90Arg
XM_017009968.2:c.268G>A	XP_016865457.1:p.Gly90Arg
XM_017009969.2:c.268G>A	XP_016865458.1:p.Gly90Arg
XM_017009970.2:c.268G>A	XP_016865459.1:p.Gly90Arg
XM_017009971.2:c.268G>A	XP_016865460.1:p.Gly90Arg
XM_017009974.2:c.268G>A	XP_016865463.1:p.Gly90Arg
NR_003149.2:n.367G>A