Canonical Allele Identifier: CA3339695
Community Standard Title: NM_032119.4(ADGRV1):c.6017G>A (p.Gly2006Asp)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90683938G>A , CM000667.2:g.90683938G>A GRCh38
NC_000005.9:g.89979755G>A , CM000667.1:g.89979755G>A GRCh37
NC_000005.8:g.90015511G>A NCBI36
NG_007083.1:g.130139G>A
NG_007083.2:g.159595G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.6017G>A MANE Select NP_115495.3:p.Gly2006Asp
ENST00000405460.9:c.6017G>A MANE Select ENSP00000384582.2:p.Gly2006Asp
NM_032119.3:c.6017G>A NP_115495.3:p.Gly2006Asp
NR_003149.1:n.6113G>A
NR_003149.2:n.6116G>A
ENST00000405460.6:c.6017G>A ENSP00000384582.2:p.Gly2006Asp
ENST00000639431.1:c.265+7729G>A ENSP00000491057.1:n.265+7729G>A
ENST00000639473.1:n.1476G>A
ENST00000640012.1:c.165-1842G>A
ENST00000640403.1:c.3308G>A ENSP00000492531.1:p.Gly1103Asp
ENST00000640779.1:c.829G>A
XM_011543675.1:c.6014G>A XP_011541977.1:p.Gly2005Asp
XM_011543676.1:c.5936G>A XP_011541978.1:p.Gly1979Asp
XM_011543677.1:c.3320G>A XP_011541979.1:p.Gly1107Asp
XM_011543678.1:c.6017G>A XP_011541980.1:p.Gly2006Asp
XM_011543679.1:c.6017G>A XP_011541981.1:p.Gly2006Asp
XM_017009963.2:c.6017G>A XP_016865452.1:p.Gly2006Asp
XM_017009964.2:c.6014G>A XP_016865453.1:p.Gly2005Asp
XM_017009965.1:c.6014G>A XP_016865454.1:p.Gly2005Asp
XM_017009966.2:c.5936G>A XP_016865455.1:p.Gly1979Asp
XM_017009967.1:c.5921G>A XP_016865456.1:p.Gly1974Asp
XM_017009968.2:c.6017G>A XP_016865457.1:p.Gly2006Asp
XM_017009969.2:c.6017G>A XP_016865458.1:p.Gly2006Asp
XM_017009970.2:c.6017G>A XP_016865459.1:p.Gly2006Asp
XM_017009971.2:c.6017G>A XP_016865460.1:p.Gly2006Asp
XM_017009973.1:c.-783G>A XP_016865462.1:n.-783G>A
XM_017009974.2:c.6017G>A XP_016865463.1:p.Gly2006Asp