Canonical Allele Identifier: CA381726763

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72108779C>G , CM000673.2:g.72108779C>G GRCh38
NC_000011.9:g.71819825C>G , CM000673.1:g.71819825C>G GRCh37
NC_000011.8:g.71497473C>G NCBI36
NG_021423.1:g.33444C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000541899.3:c.631C>G (TOMT) MANE Select ENSP00000494667.1:p.His211Asp
ENST00000541899.2:c.631C>G (TOMT) ENSP00000494667.1:p.His211Asp
ENST00000643715.1:c.*141C>G (LRTOMT) ENSP00000496019.1:n.*141C>G
ENST00000307198.11:c.730C>G (LRRC51) ENSP00000305742.7:p.His244Asp
ENST00000419228.2:c.*141C>G (LRRC51) ENSP00000392233.2:n.*141C>G
ENST00000427369.6:c.*449C>G (LRRC51) ENSP00000409403.2:n.*449C>G
ENST00000435085.5:c.730C>G (LRRC51) ENSP00000409789.1:p.His244Asp
ENST00000439209.5:c.*141C>G (LRRC51) ENSP00000395139.1:n.*141C>G
ENST00000502597.2:c.64-1174G>C (ANAPC15) ENSP00000441774.1:n.64-1174G>C
ENST00000543050.5:c.319-1174G>C (ANAPC15) ENSP00000437360.1:n.319-1174G>C
ENST00000544409.5:c.*449C>G (LRRC51) ENSP00000440969.1:n.*449C>G
NM_001145308.4:c.730C>G (LRTOMT) NP_001138780.1:p.His244Asp
NM_001145309.3:c.730C>G (LRTOMT) NP_001138781.1:p.His244Asp
NM_001145310.3:c.610C>G (LRTOMT) NP_001138782.1:p.His204Asp
XM_011544849.1:c.955C>G (LRTOMT) XP_011543151.1:p.His319Asp
NM_001330321.1:c.319-1174G>C (ANAPC15) NP_001317250.1:n.319-1174G>C
XM_024448401.1:c.955C>G (LRTOMT) XP_024304169.1:p.His319Asp
NM_001145308.5:c.730C>G (LRTOMT) NP_001138780.1:p.His244Asp
NM_001145309.4:c.730C>G (LRTOMT) NP_001138781.1:p.His244Asp
NM_001145310.4:c.610C>G (LRTOMT) NP_001138782.1:p.His204Asp
NM_001330321.2:c.319-1174G>C (ANAPC15) NP_001317250.1:n.319-1174G>C
NM_001393427.1:c.319-1174G>C (ANAPC15) NP_001380356.1:n.319-1174G>C
NM_001393428.1:c.319-1174G>C (ANAPC15) NP_001380357.1:n.319-1174G>C
NM_001393429.1:c.319-1174G>C (ANAPC15) NP_001380358.1:n.319-1174G>C
NM_001393430.1:c.319-1174G>C (ANAPC15) NP_001380359.1:n.319-1174G>C
NM_001393431.1:c.319-1174G>C (ANAPC15) NP_001380360.1:n.319-1174G>C
NM_001393443.1:c.*40G>C (ANAPC15) NP_001380372.1:n.*40G>C
NM_001393444.1:c.*40G>C (ANAPC15) NP_001380373.1:n.*40G>C
NM_001393445.1:c.*40G>C (ANAPC15) NP_001380374.1:n.*40G>C
NM_001393459.1:c.64-1174G>C (ANAPC15) NP_001380388.1:n.64-1174G>C
NM_001393500.1:c.631C>G (TOMT) NP_001380429.1:p.His211Asp
NR_171687.1:n.664G>C (ANAPC15)
NM_001393500.2:c.631C>G (TOMT) MANE Select NP_001380429.1:p.His211Asp