Canonical Allele Identifier: CA475592812

Linked Data

MyVariant Identifiers: chr11:g.71819914A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72108868A>T , CM000673.2:g.72108868A>T GRCh38
NC_000011.9:g.71819914A>T , CM000673.1:g.71819914A>T GRCh37
NC_000011.8:g.71497562A>T NCBI36
NG_021423.1:g.33533A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000541899.3:c.720A>T (TOMT) MANE Select ENSP00000494667.1:p.Pro240=
ENST00000541899.2:c.720A>T (TOMT) ENSP00000494667.1:p.Pro240=
ENST00000643715.1:c.*230A>T (LRTOMT) ENSP00000496019.1:n.*230A>T
ENST00000307198.11:c.819A>T (LRRC51) ENSP00000305742.7:p.Pro273=
ENST00000419228.2:c.*230A>T (LRRC51) ENSP00000392233.2:n.*230A>T
ENST00000427369.6:c.*538A>T (LRRC51) ENSP00000409403.2:n.*538A>T
ENST00000435085.5:c.819A>T (LRRC51) ENSP00000409789.1:p.Pro273=
ENST00000502597.2:c.63+1220T>A (ANAPC15) ENSP00000441774.1:n.63+1220T>A
ENST00000538117.5:c.*106T>A (ANAPC15) ENSP00000445212.1:n.*106T>A
ENST00000543050.5:c.318+1220T>A (ANAPC15) ENSP00000437360.1:n.318+1220T>A
ENST00000544409.5:c.*538A>T (LRRC51) ENSP00000440969.1:n.*538A>T
NM_001145308.4:c.819A>T (LRTOMT) NP_001138780.1:p.Pro273=
NM_001145309.3:c.819A>T (LRTOMT) NP_001138781.1:p.Pro273=
NM_001145310.3:c.699A>T (LRTOMT) NP_001138782.1:p.Pro233=
XM_011544849.1:c.1044A>T (LRTOMT) XP_011543151.1:p.Pro348=
NM_001330321.1:c.318+1220T>A (ANAPC15) NP_001317250.1:n.318+1220T>A
XM_024448401.1:c.1044A>T (LRTOMT) XP_024304169.1:p.Pro348=
NM_001145308.5:c.819A>T (LRTOMT) NP_001138780.1:p.Pro273=
NM_001145309.4:c.819A>T (LRTOMT) NP_001138781.1:p.Pro273=
NM_001145310.4:c.699A>T (LRTOMT) NP_001138782.1:p.Pro233=
NM_001330321.2:c.318+1220T>A (ANAPC15) NP_001317250.1:n.318+1220T>A
NM_001393427.1:c.318+1220T>A (ANAPC15) NP_001380356.1:n.318+1220T>A
NM_001393428.1:c.318+1220T>A (ANAPC15) NP_001380357.1:n.318+1220T>A
NM_001393429.1:c.318+1220T>A (ANAPC15) NP_001380358.1:n.318+1220T>A
NM_001393430.1:c.318+1220T>A (ANAPC15) NP_001380359.1:n.318+1220T>A
NM_001393431.1:c.318+1220T>A (ANAPC15) NP_001380360.1:n.318+1220T>A
NM_001393443.1:c.326T>A (ANAPC15) NP_001380372.1:p.Leu109Gln
NM_001393444.1:c.326T>A (ANAPC15) NP_001380373.1:p.Leu109Gln
NM_001393445.1:c.326T>A (ANAPC15) NP_001380374.1:p.Leu109Gln
NM_001393459.1:c.63+1220T>A (ANAPC15) NP_001380388.1:n.63+1220T>A
NM_001393500.1:c.720A>T (TOMT) NP_001380429.1:p.Pro240=
NR_171687.1:n.575T>A (ANAPC15)
NM_001393500.2:c.720A>T (TOMT) MANE Select NP_001380429.1:p.Pro240=