Canonical Allele Identifier: CA1947877338
Gene: TNNI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1840604_1840605delinsTG , CM000673.2:g.1840604_1840605delinsTG GRCh38
NC_000011.9:g.1861834_1861835delinsTG , CM000673.1:g.1861834_1861835delinsTG GRCh37
NC_000011.8:g.1818410_1818411delinsTG NCBI36
NG_011621.1:g.6602_6603delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000381911.6:c.134_135delinsTG MANE Select ENSP00000371336.1:p.Leu45=
ENST00000252898.11:c.134_135delinsTG ENSP00000252898.7:p.Leu45=
ENST00000381905.3:c.134_135delinsTG ENSP00000371330.3:p.Leu45=
ENST00000381906.5:c.134_135delinsTG ENSP00000371331.1:p.Leu45=
ENST00000381911.5:c.134_135delinsTG ENSP00000371336.1:p.Leu45=
ENST00000468473.1:n.304_305delinsTG
ENST00000617947.4:c.134_135delinsTG ENSP00000481242.1:p.Leu45=
NM_001145829.1:c.134_135delinsTG NP_001139301.1:p.Leu45=
NM_001145841.1:c.134_135delinsTG NP_001139313.1:p.Leu45=
NM_003282.3:c.134_135delinsTG NP_003273.1:p.Leu45=
NM_003282.4:c.134_135delinsTG MANE Select NP_003273.1:p.Leu45=
NM_001145829.2:c.134_135delinsTG NP_001139301.1:p.Leu45=
NM_001145841.2:c.134_135delinsTG NP_001139313.1:p.Leu45=