Canonical Allele Identifier: CA3339754
Community Standard Title: NM_032119.4(ADGRV1):c.6313A>G (p.Ile2105Val)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90685818A>G , CM000667.2:g.90685818A>G GRCh38
NC_000005.9:g.89981635A>G , CM000667.1:g.89981635A>G GRCh37
NC_000005.8:g.90017391A>G NCBI36
NG_007083.1:g.132019A>G
NG_007083.2:g.161475A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.6313A>G MANE Select NP_115495.3:p.Ile2105Val
ENST00000405460.9:c.6313A>G MANE Select ENSP00000384582.2:p.Ile2105Val
NM_032119.3:c.6313A>G NP_115495.3:p.Ile2105Val
NR_003149.1:n.6409A>G
NR_003149.2:n.6412A>G
ENST00000405460.6:c.6313A>G ENSP00000384582.2:p.Ile2105Val
ENST00000639431.1:c.265+9609A>G ENSP00000491057.1:n.265+9609A>G
ENST00000639473.1:n.1772A>G
ENST00000640012.1:c.203A>G
ENST00000640403.1:c.3604A>G ENSP00000492531.1:p.Ile1202Val
ENST00000640779.1:c.1125A>G
XM_011543675.1:c.6310A>G XP_011541977.1:p.Ile2104Val
XM_011543676.1:c.6232A>G XP_011541978.1:p.Ile2078Val
XM_011543677.1:c.3616A>G XP_011541979.1:p.Ile1206Val
XM_011543678.1:c.6313A>G XP_011541980.1:p.Ile2105Val
XM_011543679.1:c.6313A>G XP_011541981.1:p.Ile2105Val
XM_017009963.2:c.6313A>G XP_016865452.1:p.Ile2105Val
XM_017009964.2:c.6310A>G XP_016865453.1:p.Ile2104Val
XM_017009965.1:c.6310A>G XP_016865454.1:p.Ile2104Val
XM_017009966.2:c.6232A>G XP_016865455.1:p.Ile2078Val
XM_017009967.1:c.6217A>G XP_016865456.1:p.Ile2073Val
XM_017009968.2:c.6313A>G XP_016865457.1:p.Ile2105Val
XM_017009969.2:c.6313A>G XP_016865458.1:p.Ile2105Val
XM_017009970.2:c.6313A>G XP_016865459.1:p.Ile2105Val
XM_017009971.2:c.6313A>G XP_016865460.1:p.Ile2105Val
XM_017009973.1:c.-487A>G XP_016865462.1:n.-487A>G
XM_017009974.2:c.6313A>G XP_016865463.1:p.Ile2105Val