Canonical Allele Identifier: CA1981841333

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72109320C= , CM000673.2:g.72109320C= GRCh38
NC_000011.9:g.71820366C= , CM000673.1:g.71820366C= GRCh37
NC_000011.8:g.71498014C= NCBI36
NG_021423.1:g.33985C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000541899.3:c.*395C= (TOMT) MANE Select ENSP00000494667.1:n.*395C=
ENST00000541899.2:c.*395C= (TOMT) ENSP00000494667.1:n.*395C=
ENST00000307198.11:c.*395C= (LRRC51) ENSP00000305742.7:n.*395C=
ENST00000419228.2:c.*682C= (LRRC51) ENSP00000392233.2:n.*682C=
ENST00000427369.6:c.*990C= (LRRC51) ENSP00000409403.2:n.*990C=
ENST00000435085.5:c.*395C= (LRRC51) ENSP00000409789.1:n.*395C=
ENST00000502597.2:c.63+768G= (ANAPC15) ENSP00000441774.1:n.63+768G=
ENST00000538117.5:c.*7G= (ANAPC15) ENSP00000445212.1:n.*7G=
ENST00000543050.5:c.318+768G= (ANAPC15) ENSP00000437360.1:n.318+768G=
ENST00000544409.5:c.*990C= (LRRC51) ENSP00000440969.1:n.*990C=
NM_001145308.4:c.*395C= (LRTOMT) NP_001138780.1:n.*395C=
NM_001145309.3:c.*395C= (LRTOMT) NP_001138781.1:n.*395C=
NM_001145310.3:c.*395C= (LRTOMT) NP_001138782.1:n.*395C=
XM_011544849.1:c.1496C= (LRTOMT) XP_011543151.1:n.1496C=
NM_001330321.1:c.318+768G= (ANAPC15) NP_001317250.1:n.318+768G=
XM_024448401.1:c.1496C= (LRTOMT) XP_024304169.1:n.1496C=
NM_001145308.5:c.*395C= (LRTOMT) NP_001138780.1:n.*395C=
NM_001145309.4:c.*395C= (LRTOMT) NP_001138781.1:n.*395C=
NM_001145310.4:c.*395C= (LRTOMT) NP_001138782.1:n.*395C=
NM_001330321.2:c.318+768G= (ANAPC15) NP_001317250.1:n.318+768G=
NM_001393427.1:c.318+768G= (ANAPC15) NP_001380356.1:n.318+768G=
NM_001393428.1:c.318+768G= (ANAPC15) NP_001380357.1:n.318+768G=
NM_001393429.1:c.318+768G= (ANAPC15) NP_001380358.1:n.318+768G=
NM_001393430.1:c.318+768G= (ANAPC15) NP_001380359.1:n.318+768G=
NM_001393431.1:c.318+768G= (ANAPC15) NP_001380360.1:n.318+768G=
NM_001393443.1:c.319-445G= (ANAPC15) NP_001380372.1:n.319-445G=
NM_001393444.1:c.319-445G= (ANAPC15) NP_001380373.1:n.319-445G=
NM_001393445.1:c.319-445G= (ANAPC15) NP_001380374.1:n.319-445G=
NM_001393459.1:c.63+768G= (ANAPC15) NP_001380388.1:n.63+768G=
NM_001393500.1:c.*395C= (TOMT) NP_001380429.1:n.*395C=
NR_171687.1:n.476G= (ANAPC15)
NM_001393500.2:c.*395C= (TOMT) MANE Select NP_001380429.1:n.*395C=