Canonical Allele Identifier: CA475592802

Gene: TOMT LRTOMT LRRC51 ANAPC15

Linked Data

• MyVariant Identifiers: chr11:g.71819911T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72108865T>C , CM000673.2:g.72108865T>C	GRCh38
NC_000011.9:g.71819911T>C , CM000673.1:g.71819911T>C	GRCh37
NC_000011.8:g.71497559T>C	NCBI36
NG_021423.1:g.33530T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541899.3:c.717T>C (TOMT) MANE Select	ENSP00000494667.1:p.Leu239=
ENST00000541899.2:c.717T>C (TOMT)	ENSP00000494667.1:p.Leu239=
ENST00000643715.1:c.*227T>C (LRTOMT)	ENSP00000496019.1:n.*227T>C
ENST00000307198.11:c.816T>C (LRRC51)	ENSP00000305742.7:p.Leu272=
ENST00000419228.2:c.*227T>C (LRRC51)	ENSP00000392233.2:n.*227T>C
ENST00000427369.6:c.*535T>C (LRRC51)	ENSP00000409403.2:n.*535T>C
ENST00000435085.5:c.816T>C (LRRC51)	ENSP00000409789.1:p.Leu272=
ENST00000502597.2:c.63+1223A>G (ANAPC15)	ENSP00000441774.1:n.63+1223A>G
ENST00000538117.5:c.*109A>G (ANAPC15)	ENSP00000445212.1:n.*109A>G
ENST00000543050.5:c.318+1223A>G (ANAPC15)	ENSP00000437360.1:n.318+1223A>G
ENST00000544409.5:c.*535T>C (LRRC51)	ENSP00000440969.1:n.*535T>C
NM_001145308.4:c.816T>C (LRTOMT)	NP_001138780.1:p.Leu272=
NM_001145309.3:c.816T>C (LRTOMT)	NP_001138781.1:p.Leu272=
NM_001145310.3:c.696T>C (LRTOMT)	NP_001138782.1:p.Leu232=
XM_011544849.1:c.1041T>C (LRTOMT)	XP_011543151.1:p.Leu347=
NM_001330321.1:c.318+1223A>G (ANAPC15)	NP_001317250.1:n.318+1223A>G
XM_024448401.1:c.1041T>C (LRTOMT)	XP_024304169.1:p.Leu347=
NM_001145308.5:c.816T>C (LRTOMT)	NP_001138780.1:p.Leu272=
NM_001145309.4:c.816T>C (LRTOMT)	NP_001138781.1:p.Leu272=
NM_001145310.4:c.696T>C (LRTOMT)	NP_001138782.1:p.Leu232=
NM_001330321.2:c.318+1223A>G (ANAPC15)	NP_001317250.1:n.318+1223A>G
NM_001393427.1:c.318+1223A>G (ANAPC15)	NP_001380356.1:n.318+1223A>G
NM_001393428.1:c.318+1223A>G (ANAPC15)	NP_001380357.1:n.318+1223A>G
NM_001393429.1:c.318+1223A>G (ANAPC15)	NP_001380358.1:n.318+1223A>G
NM_001393430.1:c.318+1223A>G (ANAPC15)	NP_001380359.1:n.318+1223A>G
NM_001393431.1:c.318+1223A>G (ANAPC15)	NP_001380360.1:n.318+1223A>G
NM_001393443.1:c.329A>G (ANAPC15)	NP_001380372.1:p.Glu110Gly
NM_001393444.1:c.329A>G (ANAPC15)	NP_001380373.1:p.Glu110Gly
NM_001393445.1:c.329A>G (ANAPC15)	NP_001380374.1:p.Glu110Gly
NM_001393459.1:c.63+1223A>G (ANAPC15)	NP_001380388.1:n.63+1223A>G
NM_001393500.1:c.717T>C (TOMT)	NP_001380429.1:p.Leu239=
NR_171687.1:n.578A>G (ANAPC15)
NM_001393500.2:c.717T>C (TOMT) MANE Select	NP_001380429.1:p.Leu239=