Canonical Allele Identifier: CA360377354

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1445693357
• gnomAD v2: 5-90059158-G-A
• gnomAD v3: 5-90763341-G-A
• gnomAD v4: 5-90763341-G-A
• MyVariant Identifiers: chr5:g.90059158G>A (hg19) ; chr5:g.90763341G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763341G>A , CM000667.2:g.90763341G>A	GRCh38
NC_000005.9:g.90059158G>A , CM000667.1:g.90059158G>A	GRCh37
NC_000005.8:g.90094914G>A	NCBI36
NG_007083.1:g.209542G>A
NG_007083.2:g.238998G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12157G>A MANE Select	ENSP00000384582.2:p.Asp4053Asn
ENST00000425867.3:c.1111G>A	ENSP00000392618.3:p.Asp371Asn
ENST00000639431.1:c.265+87132G>A	ENSP00000491057.1:n.265+87132G>A
ENST00000640464.1:n.2576G>A
ENST00000640729.1:n.734G>A
ENST00000405460.6:c.12157G>A	ENSP00000384582.2:p.Asp4053Asn
NM_032119.3:c.12157G>A	NP_115495.3:p.Asp4053Asn
NR_003149.1:n.12170G>A
XM_011543675.1:c.12154G>A	XP_011541977.1:p.Asp4052Asn
XM_011543676.1:c.12076G>A	XP_011541978.1:p.Asp4026Asn
XM_011543677.1:c.9460G>A	XP_011541979.1:p.Asp3154Asn
XM_011543678.1:c.12157G>A	XP_011541980.1:p.Asp4053Asn
NM_032119.4:c.12157G>A MANE Select	NP_115495.3:p.Asp4053Asn
XM_017009963.2:c.12178G>A	XP_016865452.1:p.Asp4060Asn
XM_017009964.2:c.12175G>A	XP_016865453.1:p.Asp4059Asn
XM_017009965.1:c.12175G>A	XP_016865454.1:p.Asp4059Asn
XM_017009966.2:c.12097G>A	XP_016865455.1:p.Asp4033Asn
XM_017009967.1:c.12082G>A	XP_016865456.1:p.Asp4028Asn
XM_017009968.2:c.12178G>A	XP_016865457.1:p.Asp4060Asn
XM_017009969.2:c.12178G>A	XP_016865458.1:p.Asp4060Asn
XM_017009970.2:c.12178G>A	XP_016865459.1:p.Asp4060Asn
XM_017009971.2:c.12178G>A	XP_016865460.1:p.Asp4060Asn
XM_017009972.1:c.5296G>A	XP_016865461.1:p.Asp1766Asn
XM_017009973.1:c.5275G>A	XP_016865462.1:p.Asp1759Asn
NR_003149.2:n.12173G>A