Canonical Allele Identifier: CA360370956

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988466T>G (hg19) ; chr5:g.90692649T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692649T>G , CM000667.2:g.90692649T>G	GRCh38
NC_000005.9:g.89988466T>G , CM000667.1:g.89988466T>G	GRCh37
NC_000005.8:g.90024222T>G	NCBI36
NG_007083.1:g.138850T>G
NG_007083.2:g.168306T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6996T>G MANE Select	ENSP00000384582.2:p.Ile2332Met
ENST00000639431.1:c.265+16440T>G	ENSP00000491057.1:n.265+16440T>G
ENST00000639473.1:n.2455T>G
ENST00000640012.1:c.803T>G
ENST00000640374.1:n.140T>G
ENST00000640403.1:c.4287T>G	ENSP00000492531.1:p.Ile1429Met
ENST00000640779.1:c.1725T>G
ENST00000405460.6:c.6996T>G	ENSP00000384582.2:p.Ile2332Met
NM_032119.3:c.6996T>G	NP_115495.3:p.Ile2332Met
NR_003149.1:n.7009T>G
XM_011543675.1:c.6993T>G	XP_011541977.1:p.Ile2331Met
XM_011543676.1:c.6915T>G	XP_011541978.1:p.Ile2305Met
XM_011543677.1:c.4299T>G	XP_011541979.1:p.Ile1433Met
XM_011543678.1:c.6996T>G	XP_011541980.1:p.Ile2332Met
XM_011543679.1:c.6996T>G	XP_011541981.1:p.Ile2332Met
NM_032119.4:c.6996T>G MANE Select	NP_115495.3:p.Ile2332Met
XM_017009963.2:c.6996T>G	XP_016865452.1:p.Ile2332Met
XM_017009964.2:c.6993T>G	XP_016865453.1:p.Ile2331Met
XM_017009965.1:c.6993T>G	XP_016865454.1:p.Ile2331Met
XM_017009966.2:c.6915T>G	XP_016865455.1:p.Ile2305Met
XM_017009967.1:c.6900T>G	XP_016865456.1:p.Ile2300Met
XM_017009968.2:c.6996T>G	XP_016865457.1:p.Ile2332Met
XM_017009969.2:c.6996T>G	XP_016865458.1:p.Ile2332Met
XM_017009970.2:c.6996T>G	XP_016865459.1:p.Ile2332Met
XM_017009971.2:c.6996T>G	XP_016865460.1:p.Ile2332Met
XM_017009972.1:c.114T>G	XP_016865461.1:p.Ile38Met
XM_017009973.1:c.114T>G	XP_016865462.1:p.Ile38Met
XM_017009974.2:c.6996T>G	XP_016865463.1:p.Ile2332Met
NR_003149.2:n.7012T>G