Canonical Allele Identifier: CA920140592
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs1568856975

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151818_55151819insCTTG , CM000681.2:g.55151818_55151819insCTTG GRCh38
NC_000019.9:g.55663186_55663187insCTTG , CM000681.1:g.55663186_55663187insCTTG GRCh37
NC_000019.8:g.60354998_60354999insCTTG NCBI36
NG_007866.2:g.10914_10915insCAAG , LRG_432:g.10914_10915insCAAG
NG_011829.2:g.2420_2421insCAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.*15_*16insCAAG MANE Select ENSP00000341838.5:n.*15_*16insCAAG
ENST00000665070.1:c.*15_*16insCAAG ENSP00000499482.1:n.*15_*16insCAAG
ENST00000344887.9:c.*15_*16insCAAG ENSP00000341838.5:n.*15_*16insCAAG
ENST00000585806.5:n.647_648insCAAG
ENST00000588882.1:c.*15_*16insCAAG ENSP00000466729.1:n.*15_*16insCAAG
ENST00000589864.1:n.476_477insCAAG
NM_000363.4:c.*15_*16insCAAG , LRG_432t1:c.*15_*16insCAAG NP_000354.4:n.*15_*16insCAAG
NM_000363.5:c.*15_*16insCAAG MANE Select NP_000354.4:n.*15_*16insCAAG