Canonical Allele Identifier: CA1562882065
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90745610G= , CM000667.2:g.90745610G= GRCh38
NC_000005.9:g.90041427G= , CM000667.1:g.90041427G= GRCh37
NC_000005.8:g.90077183G= NCBI36
NG_007083.1:g.191811G=
NG_007083.2:g.221267G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.10789G= MANE Select ENSP00000384582.2:p.Glu3597=
ENST00000639431.1:c.265+69401G= ENSP00000491057.1:n.265+69401G=
ENST00000640374.1:n.3933G=
ENST00000640464.1:n.1208G=
ENST00000405460.6:c.10789G= ENSP00000384582.2:p.Glu3597=
ENST00000509621.1:c.3486G=
NM_032119.3:c.10789G= NP_115495.3:p.Glu3597=
NR_003149.1:n.10802G=
XM_011543675.1:c.10786G= XP_011541977.1:p.Glu3596=
XM_011543676.1:c.10708G= XP_011541978.1:p.Glu3570=
XM_011543677.1:c.8092G= XP_011541979.1:p.Glu2698=
XM_011543678.1:c.10789G= XP_011541980.1:p.Glu3597=
XM_011543679.1:c.*11G= XP_011541981.1:n.*11G=
NM_032119.4:c.10789G= MANE Select NP_115495.3:p.Glu3597=
XM_017009963.2:c.10810G= XP_016865452.1:p.Glu3604=
XM_017009964.2:c.10807G= XP_016865453.1:p.Glu3603=
XM_017009965.1:c.10807G= XP_016865454.1:p.Glu3603=
XM_017009966.2:c.10729G= XP_016865455.1:p.Glu3577=
XM_017009967.1:c.10714G= XP_016865456.1:p.Glu3572=
XM_017009968.2:c.10810G= XP_016865457.1:p.Glu3604=
XM_017009969.2:c.10810G= XP_016865458.1:p.Glu3604=
XM_017009970.2:c.10810G= XP_016865459.1:p.Glu3604=
XM_017009971.2:c.10810G= XP_016865460.1:p.Glu3604=
XM_017009972.1:c.3928G= XP_016865461.1:p.Glu1310=
XM_017009973.1:c.3907G= XP_016865462.1:p.Glu1303=
XM_017009974.2:c.*11G= XP_016865463.1:n.*11G=
NR_003149.2:n.10805G=