Canonical Allele Identifier: CA360402199

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791325C>G , CM000667.2:g.90791325C>G	GRCh38
NC_000005.9:g.90087142C>G , CM000667.1:g.90087142C>G	GRCh37
NC_000005.8:g.90122898C>G	NCBI36
NG_007083.1:g.237526C>G
NG_007083.2:g.266982C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14496C>G MANE Select	NP_115495.3:p.Asp4832Glu
ENST00000405460.9:c.14496C>G MANE Select	ENSP00000384582.2:p.Asp4832Glu
NM_032119.3:c.14496C>G	NP_115495.3:p.Asp4832Glu
NR_003149.1:n.14509C>G
NR_003149.2:n.14512C>G
ENST00000405460.6:c.14496C>G	ENSP00000384582.2:p.Asp4832Glu
ENST00000425867.2:c.1479C>G	ENSP00000392618.2:p.Asp493Glu
ENST00000425867.3:c.3450C>G	ENSP00000392618.3:p.Asp1150Glu
ENST00000507314.1:n.171C>G
ENST00000507314.2:c.171C>G	ENSP00000491299.1:p.Asp57Glu
ENST00000638510.1:n.1763C>G
ENST00000638585.1:n.262C>G
ENST00000638975.1:c.1125C>G	ENSP00000492630.1:p.Asp375Glu
ENST00000639431.1:c.265+115116C>G	ENSP00000491057.1:n.265+115116C>G
ENST00000640407.1:c.906C>G	ENSP00000491425.1:p.Asp302Glu
XM_011543675.1:c.14493C>G	XP_011541977.1:p.Asp4831Glu
XM_011543676.1:c.14415C>G	XP_011541978.1:p.Asp4805Glu
XM_011543677.1:c.11799C>G	XP_011541979.1:p.Asp3933Glu
XM_011543678.1:c.14496C>G	XP_011541980.1:p.Asp4832Glu
XM_017009963.2:c.14517C>G	XP_016865452.1:p.Asp4839Glu
XM_017009964.2:c.14514C>G	XP_016865453.1:p.Asp4838Glu
XM_017009965.1:c.14514C>G	XP_016865454.1:p.Asp4838Glu
XM_017009966.2:c.14436C>G	XP_016865455.1:p.Asp4812Glu
XM_017009967.1:c.14421C>G	XP_016865456.1:p.Asp4807Glu
XM_017009968.2:c.14517C>G	XP_016865457.1:p.Asp4839Glu
XM_017009969.2:c.14517C>G	XP_016865458.1:p.Asp4839Glu
XM_017009970.2:c.14517C>G	XP_016865459.1:p.Asp4839Glu
XM_017009971.2:c.14517C>G	XP_016865460.1:p.Asp4839Glu
XM_017009972.1:c.7635C>G	XP_016865461.1:p.Asp2545Glu
XM_017009973.1:c.7614C>G	XP_016865462.1:p.Asp2538Glu