Canonical Allele Identifier: CA360401272

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1222025537
• gnomAD v4: 5-90791106-C-A
• MyVariant Identifiers: chr5:g.90086923C>A (hg19) ; chr5:g.90791106C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791106C>A , CM000667.2:g.90791106C>A	GRCh38
NC_000005.9:g.90086923C>A , CM000667.1:g.90086923C>A	GRCh37
NC_000005.8:g.90122679C>A	NCBI36
NG_007083.1:g.237307C>A
NG_007083.2:g.266763C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14277C>A MANE Select	ENSP00000384582.2:p.Asp4759Glu
ENST00000425867.3:c.3231C>A	ENSP00000392618.3:p.Asp1077Glu
ENST00000638510.1:n.1544C>A
ENST00000638585.1:n.43C>A
ENST00000638975.1:c.906C>A	ENSP00000492630.1:p.Asp302Glu
ENST00000639431.1:c.265+114897C>A	ENSP00000491057.1:n.265+114897C>A
ENST00000640407.1:c.687C>A	ENSP00000491425.1:p.Asp229Glu
ENST00000405460.6:c.14277C>A	ENSP00000384582.2:p.Asp4759Glu
ENST00000425867.2:c.1260C>A	ENSP00000392618.2:p.Asp420Glu
NM_032119.3:c.14277C>A	NP_115495.3:p.Asp4759Glu
NR_003149.1:n.14290C>A
XM_011543675.1:c.14274C>A	XP_011541977.1:p.Asp4758Glu
XM_011543676.1:c.14196C>A	XP_011541978.1:p.Asp4732Glu
XM_011543677.1:c.11580C>A	XP_011541979.1:p.Asp3860Glu
XM_011543678.1:c.14277C>A	XP_011541980.1:p.Asp4759Glu
NM_032119.4:c.14277C>A MANE Select	NP_115495.3:p.Asp4759Glu
XM_017009963.2:c.14298C>A	XP_016865452.1:p.Asp4766Glu
XM_017009964.2:c.14295C>A	XP_016865453.1:p.Asp4765Glu
XM_017009965.1:c.14295C>A	XP_016865454.1:p.Asp4765Glu
XM_017009966.2:c.14217C>A	XP_016865455.1:p.Asp4739Glu
XM_017009967.1:c.14202C>A	XP_016865456.1:p.Asp4734Glu
XM_017009968.2:c.14298C>A	XP_016865457.1:p.Asp4766Glu
XM_017009969.2:c.14298C>A	XP_016865458.1:p.Asp4766Glu
XM_017009970.2:c.14298C>A	XP_016865459.1:p.Asp4766Glu
XM_017009971.2:c.14298C>A	XP_016865460.1:p.Asp4766Glu
XM_017009972.1:c.7416C>A	XP_016865461.1:p.Asp2472Glu
XM_017009973.1:c.7395C>A	XP_016865462.1:p.Asp2465Glu
NR_003149.2:n.14293C>A