Canonical Allele Identifier: CA1981841023

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72108618T= , CM000673.2:g.72108618T= GRCh38
NC_000011.9:g.71819664T= , CM000673.1:g.71819664T= GRCh37
NC_000011.8:g.71497312T= NCBI36
NG_021423.1:g.33283T=

Transcript Alleles

HGVS Amino-acid change
ENST00000541899.3:c.470T= (TOMT) MANE Select ENSP00000494667.1:p.Val157=
ENST00000541899.2:c.470T= (TOMT) ENSP00000494667.1:p.Val157=
ENST00000643715.1:c.451T= (LRTOMT) ENSP00000496019.1:p.Trp151=
ENST00000307198.11:c.569T= (LRRC51) ENSP00000305742.7:p.Val190=
ENST00000419228.2:c.448T= (LRRC51) ENSP00000392233.2:p.Trp150=
ENST00000427369.6:c.*288T= (LRRC51) ENSP00000409403.2:n.*288T=
ENST00000435085.5:c.569T= (LRRC51) ENSP00000409789.1:p.Val190=
ENST00000439209.5:c.451T= (LRRC51) ENSP00000395139.1:p.Trp151=
ENST00000502597.2:c.64-1013A= (ANAPC15) ENSP00000441774.1:n.64-1013A=
ENST00000543050.5:c.319-1013A= (ANAPC15) ENSP00000437360.1:n.319-1013A=
ENST00000544409.5:c.*288T= (LRRC51) ENSP00000440969.1:n.*288T=
NM_001145308.4:c.569T= (LRTOMT) NP_001138780.1:p.Val190=
NM_001145309.3:c.569T= (LRTOMT) NP_001138781.1:p.Val190=
NM_001145310.3:c.449T= (LRTOMT) NP_001138782.1:p.Val150=
XM_011544849.1:c.794T= (LRTOMT) XP_011543151.1:p.Val265=
NM_001330321.1:c.319-1013A= (ANAPC15) NP_001317250.1:n.319-1013A=
XM_024448401.1:c.794T= (LRTOMT) XP_024304169.1:p.Val265=
NM_001145308.5:c.569T= (LRTOMT) NP_001138780.1:p.Val190=
NM_001145309.4:c.569T= (LRTOMT) NP_001138781.1:p.Val190=
NM_001145310.4:c.449T= (LRTOMT) NP_001138782.1:p.Val150=
NM_001330321.2:c.319-1013A= (ANAPC15) NP_001317250.1:n.319-1013A=
NM_001393427.1:c.319-1013A= (ANAPC15) NP_001380356.1:n.319-1013A=
NM_001393428.1:c.319-1013A= (ANAPC15) NP_001380357.1:n.319-1013A=
NM_001393429.1:c.319-1013A= (ANAPC15) NP_001380358.1:n.319-1013A=
NM_001393430.1:c.319-1013A= (ANAPC15) NP_001380359.1:n.319-1013A=
NM_001393431.1:c.319-1013A= (ANAPC15) NP_001380360.1:n.319-1013A=
NM_001393443.1:c.*201A= (ANAPC15) NP_001380372.1:n.*201A=
NM_001393444.1:c.*201A= (ANAPC15) NP_001380373.1:n.*201A=
NM_001393445.1:c.*201A= (ANAPC15) NP_001380374.1:n.*201A=
NM_001393459.1:c.64-1013A= (ANAPC15) NP_001380388.1:n.64-1013A=
NM_001393500.1:c.470T= (TOMT) NP_001380429.1:p.Val157=
NR_171687.1:n.825A= (ANAPC15)
NM_001393500.2:c.470T= (TOMT) MANE Select NP_001380429.1:p.Val157=