Canonical Allele Identifier: CA122388
Community Standard Title: NM_003282.4(TNNI2):c.499_501del (p.Glu167del)
Gene: TNNI2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1841501_1841503del , CM000673.2:g.1841501_1841503del GRCh38
NC_000011.9:g.1862731_1862733del , CM000673.1:g.1862731_1862733del GRCh37
NC_000011.8:g.1819307_1819309del NCBI36
NG_011621.1:g.7499_7501del

Transcript Alleles

HGVS Amino-acid Change
NM_003282.4:c.499_501del MANE Select NP_003273.1:p.Glu167del
ENST00000381911.6:c.499_501del MANE Select ENSP00000371336.1:p.Glu167del
NM_001145829.1:c.499_501del NP_001139301.1:p.Glu167del
NM_001145829.2:c.499_501del NP_001139301.1:p.Glu167del
NM_001145841.1:c.499_501del NP_001139313.1:p.Glu167del
NM_001145841.2:c.499_501del NP_001139313.1:p.Glu167del
NM_003282.3:c.499_501del NP_003273.1:p.Glu167del
ENST00000252898.11:c.499_501del ENSP00000252898.7:p.Glu167del
ENST00000381905.3:c.499_501del ENSP00000371330.3:p.Glu167del
ENST00000381906.5:c.499_501del ENSP00000371331.1:p.Glu167del
ENST00000381911.5:c.499_501del ENSP00000371336.1:p.Glu167del
ENST00000617947.4:c.499_501del ENSP00000481242.1:p.Glu167del
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