Canonical Allele Identifier: CA360371146

Gene: ADGRV1

Linked Data

• COSMIC: COSM3140674
• MyVariant Identifiers: chr5:g.89988490T>G (hg19) ; chr5:g.90692673T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692673T>G , CM000667.2:g.90692673T>G	GRCh38
NC_000005.9:g.89988490T>G , CM000667.1:g.89988490T>G	GRCh37
NC_000005.8:g.90024246T>G	NCBI36
NG_007083.1:g.138874T>G
NG_007083.2:g.168330T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7020T>G MANE Select	ENSP00000384582.2:p.Ile2340Met
ENST00000639431.1:c.265+16464T>G	ENSP00000491057.1:n.265+16464T>G
ENST00000639473.1:n.2479T>G
ENST00000640012.1:c.827T>G
ENST00000640374.1:n.164T>G
ENST00000640403.1:c.4311T>G	ENSP00000492531.1:p.Ile1437Met
ENST00000640779.1:c.1749T>G
ENST00000405460.6:c.7020T>G	ENSP00000384582.2:p.Ile2340Met
NM_032119.3:c.7020T>G	NP_115495.3:p.Ile2340Met
NR_003149.1:n.7033T>G
XM_011543675.1:c.7017T>G	XP_011541977.1:p.Ile2339Met
XM_011543676.1:c.6939T>G	XP_011541978.1:p.Ile2313Met
XM_011543677.1:c.4323T>G	XP_011541979.1:p.Ile1441Met
XM_011543678.1:c.7020T>G	XP_011541980.1:p.Ile2340Met
XM_011543679.1:c.7020T>G	XP_011541981.1:p.Ile2340Met
NM_032119.4:c.7020T>G MANE Select	NP_115495.3:p.Ile2340Met
XM_017009963.2:c.7020T>G	XP_016865452.1:p.Ile2340Met
XM_017009964.2:c.7017T>G	XP_016865453.1:p.Ile2339Met
XM_017009965.1:c.7017T>G	XP_016865454.1:p.Ile2339Met
XM_017009966.2:c.6939T>G	XP_016865455.1:p.Ile2313Met
XM_017009967.1:c.6924T>G	XP_016865456.1:p.Ile2308Met
XM_017009968.2:c.7020T>G	XP_016865457.1:p.Ile2340Met
XM_017009969.2:c.7020T>G	XP_016865458.1:p.Ile2340Met
XM_017009970.2:c.7020T>G	XP_016865459.1:p.Ile2340Met
XM_017009971.2:c.7020T>G	XP_016865460.1:p.Ile2340Met
XM_017009972.1:c.138T>G	XP_016865461.1:p.Ile46Met
XM_017009973.1:c.138T>G	XP_016865462.1:p.Ile46Met
XM_017009974.2:c.7020T>G	XP_016865463.1:p.Ile2340Met
NR_003149.2:n.7036T>G