Canonical Allele Identifier: CA1947877342
Gene: TNNI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1840607_1840609delinsCGG , CM000673.2:g.1840607_1840609delinsCGG GRCh38
NC_000011.9:g.1861837_1861839delinsCGG , CM000673.1:g.1861837_1861839delinsCGG GRCh37
NC_000011.8:g.1818413_1818415delinsCGG NCBI36
NG_011621.1:g.6605_6607delinsCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000381911.6:c.137_139delinsCGG MANE Select ENSP00000371336.1:p.Ala46=
ENST00000252898.11:c.137_139delinsCGG ENSP00000252898.7:p.Ala46=
ENST00000381905.3:c.137_139delinsCGG ENSP00000371330.3:p.Ala46=
ENST00000381906.5:c.137_139delinsCGG ENSP00000371331.1:p.Ala46=
ENST00000381911.5:c.137_139delinsCGG ENSP00000371336.1:p.Ala46=
ENST00000468473.1:n.307_309delinsCGG
ENST00000617947.4:c.137_139delinsCGG ENSP00000481242.1:p.Ala46=
NM_001145829.1:c.137_139delinsCGG NP_001139301.1:p.Ala46=
NM_001145841.1:c.137_139delinsCGG NP_001139313.1:p.Ala46=
NM_003282.3:c.137_139delinsCGG NP_003273.1:p.Ala46=
NM_003282.4:c.137_139delinsCGG MANE Select NP_003273.1:p.Ala46=
NM_001145829.2:c.137_139delinsCGG NP_001139301.1:p.Ala46=
NM_001145841.2:c.137_139delinsCGG NP_001139313.1:p.Ala46=