Canonical Allele Identifier: CA561259792

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1267254042
• gnomAD v2: 5-89989657-A-G
• gnomAD v4: 5-90693840-A-G
• MyVariant Identifiers: chr5:g.89989657A>G (hg19) ; chr5:g.90693840A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90693840A>G , CM000667.2:g.90693840A>G	GRCh38
NC_000005.9:g.89989657A>G , CM000667.1:g.89989657A>G	GRCh37
NC_000005.8:g.90025413A>G	NCBI36
NG_007083.1:g.140041A>G
NG_007083.2:g.169497A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7134-50A>G MANE Select	ENSP00000384582.2:n.7134-50A>G
ENST00000639431.1:c.265+17631A>G	ENSP00000491057.1:n.265+17631A>G
ENST00000639473.1:n.2593-50A>G
ENST00000640012.1:c.941-50A>G
ENST00000640374.1:n.278-50A>G
ENST00000640403.1:c.4425-50A>G	ENSP00000492531.1:n.4425-50A>G
ENST00000640779.1:c.1863-50A>G
ENST00000405460.6:c.7134-50A>G	ENSP00000384582.2:n.7134-50A>G
NM_032119.3:c.7134-50A>G	NP_115495.3:n.7134-50A>G
NR_003149.1:n.7147-50A>G
XM_011543675.1:c.7131-50A>G	XP_011541977.1:n.7131-50A>G
XM_011543676.1:c.7053-50A>G	XP_011541978.1:n.7053-50A>G
XM_011543677.1:c.4437-50A>G	XP_011541979.1:n.4437-50A>G
XM_011543678.1:c.7134-50A>G	XP_011541980.1:n.7134-50A>G
XM_011543679.1:c.7134-50A>G	XP_011541981.1:n.7134-50A>G
NM_032119.4:c.7134-50A>G MANE Select	NP_115495.3:n.7134-50A>G
XM_017009963.2:c.7134-50A>G	XP_016865452.1:n.7134-50A>G
XM_017009964.2:c.7131-50A>G	XP_016865453.1:n.7131-50A>G
XM_017009965.1:c.7131-50A>G	XP_016865454.1:n.7131-50A>G
XM_017009966.2:c.7053-50A>G	XP_016865455.1:n.7053-50A>G
XM_017009967.1:c.7038-50A>G	XP_016865456.1:n.7038-50A>G
XM_017009968.2:c.7134-50A>G	XP_016865457.1:n.7134-50A>G
XM_017009969.2:c.7134-50A>G	XP_016865458.1:n.7134-50A>G
XM_017009970.2:c.7134-50A>G	XP_016865459.1:n.7134-50A>G
XM_017009971.2:c.7134-50A>G	XP_016865460.1:n.7134-50A>G
XM_017009972.1:c.252-50A>G	XP_016865461.1:n.252-50A>G
XM_017009973.1:c.252-50A>G	XP_016865462.1:n.252-50A>G
XM_017009974.2:c.7134-50A>G	XP_016865463.1:n.7134-50A>G
NR_003149.2:n.7150-50A>G