Canonical Allele Identifier: CA3338576

Gene: ADGRV1

Linked Data

• ClinVar Variation Id: 2820260
• ClinVar RCV Id: RCV003709097
• dbSNP Id: rs570861759
• ExAC: 5:89923220 A / G
• gnomAD v2: 5-89923220-A-G
• gnomAD v3: 5-90627403-A-G
• gnomAD v4: 5-90627403-A-G
• MyVariant Identifiers: chr5:g.89923220A>G (hg19) ; chr5:g.90627403A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627403A>G , CM000667.2:g.90627403A>G	GRCh38
NC_000005.9:g.89923220A>G , CM000667.1:g.89923220A>G	GRCh37
NC_000005.8:g.89958976A>G	NCBI36
NG_007083.1:g.73604A>G
NG_007083.2:g.103060A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.865A>G MANE Select	ENSP00000384582.2:p.Asn289Asp
ENST00000640083.1:n.570A>G
ENST00000640109.1:n.961A>G
ENST00000640281.1:n.924A>G
ENST00000405460.6:c.865A>G	ENSP00000384582.2:p.Asn289Asp
NM_032119.3:c.865A>G	NP_115495.3:p.Asn289Asp
NR_003149.1:n.961A>G
XM_011543675.1:c.865A>G	XP_011541977.1:p.Asn289Asp
XM_011543676.1:c.865A>G	XP_011541978.1:p.Asn289Asp
XM_011543678.1:c.865A>G	XP_011541980.1:p.Asn289Asp
XM_011543679.1:c.865A>G	XP_011541981.1:p.Asn289Asp
NM_032119.4:c.865A>G MANE Select	NP_115495.3:p.Asn289Asp
XM_017009963.2:c.865A>G	XP_016865452.1:p.Asn289Asp
XM_017009964.2:c.865A>G	XP_016865453.1:p.Asn289Asp
XM_017009965.1:c.862A>G	XP_016865454.1:p.Asn288Asp
XM_017009966.2:c.865A>G	XP_016865455.1:p.Asn289Asp
XM_017009967.1:c.769A>G	XP_016865456.1:p.Asn257Asp
XM_017009968.2:c.865A>G	XP_016865457.1:p.Asn289Asp
XM_017009969.2:c.865A>G	XP_016865458.1:p.Asn289Asp
XM_017009970.2:c.865A>G	XP_016865459.1:p.Asn289Asp
XM_017009971.2:c.865A>G	XP_016865460.1:p.Asn289Asp
XM_017009974.2:c.865A>G	XP_016865463.1:p.Asn289Asp
NR_003149.2:n.964A>G