Canonical Allele Identifier: CA3340878
Community Standard Title: NM_032119.4(ADGRV1):c.10997A>G (p.Glu3666Gly)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90750573A>G , CM000667.2:g.90750573A>G GRCh38
NC_000005.9:g.90046390A>G , CM000667.1:g.90046390A>G GRCh37
NC_000005.8:g.90082146A>G NCBI36
NG_007083.1:g.196774A>G
NG_007083.2:g.226230A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.10997A>G MANE Select NP_115495.3:p.Glu3666Gly
ENST00000405460.9:c.10997A>G MANE Select ENSP00000384582.2:p.Glu3666Gly
NM_032119.3:c.10997A>G NP_115495.3:p.Glu3666Gly
NR_003149.1:n.11010A>G
NR_003149.2:n.11013A>G
ENST00000405460.6:c.10997A>G ENSP00000384582.2:p.Glu3666Gly
ENST00000425867.3:c.128A>G ENSP00000392618.3:p.Glu43Gly
ENST00000509621.1:c.3694A>G
ENST00000639431.1:c.265+74364A>G ENSP00000491057.1:n.265+74364A>G
ENST00000640374.1:n.4141A>G
ENST00000640464.1:n.1416A>G
XM_011543675.1:c.10994A>G XP_011541977.1:p.Glu3665Gly
XM_011543676.1:c.10916A>G XP_011541978.1:p.Glu3639Gly
XM_011543677.1:c.8300A>G XP_011541979.1:p.Glu2767Gly
XM_011543678.1:c.10997A>G XP_011541980.1:p.Glu3666Gly
XM_017009963.2:c.11018A>G XP_016865452.1:p.Glu3673Gly
XM_017009964.2:c.11015A>G XP_016865453.1:p.Glu3672Gly
XM_017009965.1:c.11015A>G XP_016865454.1:p.Glu3672Gly
XM_017009966.2:c.10937A>G XP_016865455.1:p.Glu3646Gly
XM_017009967.1:c.10922A>G XP_016865456.1:p.Glu3641Gly
XM_017009968.2:c.11018A>G XP_016865457.1:p.Glu3673Gly
XM_017009969.2:c.11018A>G XP_016865458.1:p.Glu3673Gly
XM_017009970.2:c.11018A>G XP_016865459.1:p.Glu3673Gly
XM_017009971.2:c.11018A>G XP_016865460.1:p.Glu3673Gly
XM_017009972.1:c.4136A>G XP_016865461.1:p.Glu1379Gly
XM_017009973.1:c.4115A>G XP_016865462.1:p.Glu1372Gly