Canonical Allele Identifier: CA360371209

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988496T>G (hg19) ; chr5:g.90692679T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692679T>G , CM000667.2:g.90692679T>G	GRCh38
NC_000005.9:g.89988496T>G , CM000667.1:g.89988496T>G	GRCh37
NC_000005.8:g.90024252T>G	NCBI36
NG_007083.1:g.138880T>G
NG_007083.2:g.168336T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7026T>G MANE Select	ENSP00000384582.2:p.Ile2342Met
ENST00000639431.1:c.265+16470T>G	ENSP00000491057.1:n.265+16470T>G
ENST00000639473.1:n.2485T>G
ENST00000640012.1:c.833T>G
ENST00000640374.1:n.170T>G
ENST00000640403.1:c.4317T>G	ENSP00000492531.1:p.Ile1439Met
ENST00000640779.1:c.1755T>G
ENST00000405460.6:c.7026T>G	ENSP00000384582.2:p.Ile2342Met
NM_032119.3:c.7026T>G	NP_115495.3:p.Ile2342Met
NR_003149.1:n.7039T>G
XM_011543675.1:c.7023T>G	XP_011541977.1:p.Ile2341Met
XM_011543676.1:c.6945T>G	XP_011541978.1:p.Ile2315Met
XM_011543677.1:c.4329T>G	XP_011541979.1:p.Ile1443Met
XM_011543678.1:c.7026T>G	XP_011541980.1:p.Ile2342Met
XM_011543679.1:c.7026T>G	XP_011541981.1:p.Ile2342Met
NM_032119.4:c.7026T>G MANE Select	NP_115495.3:p.Ile2342Met
XM_017009963.2:c.7026T>G	XP_016865452.1:p.Ile2342Met
XM_017009964.2:c.7023T>G	XP_016865453.1:p.Ile2341Met
XM_017009965.1:c.7023T>G	XP_016865454.1:p.Ile2341Met
XM_017009966.2:c.6945T>G	XP_016865455.1:p.Ile2315Met
XM_017009967.1:c.6930T>G	XP_016865456.1:p.Ile2310Met
XM_017009968.2:c.7026T>G	XP_016865457.1:p.Ile2342Met
XM_017009969.2:c.7026T>G	XP_016865458.1:p.Ile2342Met
XM_017009970.2:c.7026T>G	XP_016865459.1:p.Ile2342Met
XM_017009971.2:c.7026T>G	XP_016865460.1:p.Ile2342Met
XM_017009972.1:c.144T>G	XP_016865461.1:p.Ile48Met
XM_017009973.1:c.144T>G	XP_016865462.1:p.Ile48Met
XM_017009974.2:c.7026T>G	XP_016865463.1:p.Ile2342Met
NR_003149.2:n.7042T>G