Canonical Allele Identifier: CA883720719

Gene: TNNI3

Linked Data

• dbSNP Id: rs1208458716
• gnomAD v3: 19-55152246-TG-T
• gnomAD v4: 19-55152246-TG-T
• MyVariant Identifiers: chr19:g.55663615del (hg19) ; chr19:g.55152247del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152247del , CM000681.2:g.55152247del	GRCh38
NC_000019.9:g.55663615del , CM000681.1:g.55663615del	GRCh37
NC_000019.8:g.60355427del	NCBI36
NG_007866.2:g.10486del , LRG_432:g.10486del
NG_011829.2:g.1992del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-330del MANE Select	ENSP00000341838.5:n.550-330del
ENST00000665070.1:c.583-330del	ENSP00000499482.1:n.583-330del
ENST00000344887.9:c.550-330del	ENSP00000341838.5:n.550-330del
ENST00000585806.5:n.549-330del
ENST00000588882.1:c.475-330del	ENSP00000466729.1:n.475-330del
ENST00000589864.1:n.378-330del
NM_000363.4:c.550-330del , LRG_432t1:c.550-330del	NP_000354.4:n.550-330del
NM_000363.5:c.550-330del MANE Select	NP_000354.4:n.550-330del