Canonical Allele Identifier: CA360388768

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89999505A>G (hg19) ; chr5:g.90703688A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703688A>G , CM000667.2:g.90703688A>G	GRCh38
NC_000005.9:g.89999505A>G , CM000667.1:g.89999505A>G	GRCh37
NC_000005.8:g.90035261A>G	NCBI36
NG_007083.1:g.149889A>G
NG_007083.2:g.179345A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.8179A>G MANE Select	ENSP00000384582.2:p.Ile2727Val
ENST00000639431.1:c.265+27479A>G	ENSP00000491057.1:n.265+27479A>G
ENST00000639473.1:n.3638A>G
ENST00000640012.1:c.1986A>G
ENST00000640374.1:n.1323A>G
ENST00000640403.1:c.5470A>G	ENSP00000492531.1:p.Ile1824Val
ENST00000640779.1:c.2908A>G
ENST00000405460.6:c.8179A>G	ENSP00000384582.2:p.Ile2727Val
ENST00000509621.1:c.876A>G
NM_032119.3:c.8179A>G	NP_115495.3:p.Ile2727Val
NR_003149.1:n.8192A>G
XM_011543675.1:c.8176A>G	XP_011541977.1:p.Ile2726Val
XM_011543676.1:c.8098A>G	XP_011541978.1:p.Ile2700Val
XM_011543677.1:c.5482A>G	XP_011541979.1:p.Ile1828Val
XM_011543678.1:c.8179A>G	XP_011541980.1:p.Ile2727Val
XM_011543679.1:c.8179A>G	XP_011541981.1:p.Ile2727Val
NM_032119.4:c.8179A>G MANE Select	NP_115495.3:p.Ile2727Val
XM_017009963.2:c.8179A>G	XP_016865452.1:p.Ile2727Val
XM_017009964.2:c.8176A>G	XP_016865453.1:p.Ile2726Val
XM_017009965.1:c.8176A>G	XP_016865454.1:p.Ile2726Val
XM_017009966.2:c.8098A>G	XP_016865455.1:p.Ile2700Val
XM_017009967.1:c.8083A>G	XP_016865456.1:p.Ile2695Val
XM_017009968.2:c.8179A>G	XP_016865457.1:p.Ile2727Val
XM_017009969.2:c.8179A>G	XP_016865458.1:p.Ile2727Val
XM_017009970.2:c.8179A>G	XP_016865459.1:p.Ile2727Val
XM_017009971.2:c.8179A>G	XP_016865460.1:p.Ile2727Val
XM_017009972.1:c.1297A>G	XP_016865461.1:p.Ile433Val
XM_017009973.1:c.1297A>G	XP_016865462.1:p.Ile433Val
XM_017009974.2:c.8179A>G	XP_016865463.1:p.Ile2727Val
NR_003149.2:n.8195A>G