Canonical Allele Identifier: CA2695229162
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154775del , CM000681.2:g.55154775del GRCh38
NC_000019.9:g.55666143del , CM000681.1:g.55666143del GRCh37
NC_000019.8:g.60357955del NCBI36
NG_007866.2:g.7958del , LRG_432:g.7958del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.338del MANE Select ENSP00000341838.5:p.Asp113AlafsTer2
ENST00000665070.1:c.338del ENSP00000499482.1:p.Asp113AlafsTer2
ENST00000344887.9:c.338del ENSP00000341838.5:p.Asp113AlafsTer2
ENST00000585806.5:n.337del
ENST00000586669.5:n.346del
ENST00000587176.5:n.522del
ENST00000587871.1:c.957del
ENST00000588882.1:c.263del ENSP00000466729.1:p.Asp88AlafsTer2
ENST00000590463.1:n.510del
NM_000363.4:c.338del , LRG_432t1:c.338del NP_000354.4:p.Asp113AlafsTer2
NM_000363.5:c.338del MANE Select NP_000354.4:p.Asp113AlafsTer2