Canonical Allele Identifier: CA360377386

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059159A>G (hg19) ; chr5:g.90763342A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763342A>G , CM000667.2:g.90763342A>G	GRCh38
NC_000005.9:g.90059159A>G , CM000667.1:g.90059159A>G	GRCh37
NC_000005.8:g.90094915A>G	NCBI36
NG_007083.1:g.209543A>G
NG_007083.2:g.238999A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12158A>G MANE Select	ENSP00000384582.2:p.Asp4053Gly
ENST00000425867.3:c.1112A>G	ENSP00000392618.3:p.Asp371Gly
ENST00000639431.1:c.265+87133A>G	ENSP00000491057.1:n.265+87133A>G
ENST00000640464.1:n.2577A>G
ENST00000640729.1:n.735A>G
ENST00000405460.6:c.12158A>G	ENSP00000384582.2:p.Asp4053Gly
NM_032119.3:c.12158A>G	NP_115495.3:p.Asp4053Gly
NR_003149.1:n.12171A>G
XM_011543675.1:c.12155A>G	XP_011541977.1:p.Asp4052Gly
XM_011543676.1:c.12077A>G	XP_011541978.1:p.Asp4026Gly
XM_011543677.1:c.9461A>G	XP_011541979.1:p.Asp3154Gly
XM_011543678.1:c.12158A>G	XP_011541980.1:p.Asp4053Gly
NM_032119.4:c.12158A>G MANE Select	NP_115495.3:p.Asp4053Gly
XM_017009963.2:c.12179A>G	XP_016865452.1:p.Asp4060Gly
XM_017009964.2:c.12176A>G	XP_016865453.1:p.Asp4059Gly
XM_017009965.1:c.12176A>G	XP_016865454.1:p.Asp4059Gly
XM_017009966.2:c.12098A>G	XP_016865455.1:p.Asp4033Gly
XM_017009967.1:c.12083A>G	XP_016865456.1:p.Asp4028Gly
XM_017009968.2:c.12179A>G	XP_016865457.1:p.Asp4060Gly
XM_017009969.2:c.12179A>G	XP_016865458.1:p.Asp4060Gly
XM_017009970.2:c.12179A>G	XP_016865459.1:p.Asp4060Gly
XM_017009971.2:c.12179A>G	XP_016865460.1:p.Asp4060Gly
XM_017009972.1:c.5297A>G	XP_016865461.1:p.Asp1766Gly
XM_017009973.1:c.5276A>G	XP_016865462.1:p.Asp1759Gly
NR_003149.2:n.12174A>G