Canonical Allele Identifier: CA2580097803

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 1747856
• ClinVar RCV Id: RCV002351546

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154026_55154029del , CM000681.2:g.55154026_55154029del	GRCh38
NC_000019.9:g.55665394_55665397del , CM000681.1:g.55665394_55665397del	GRCh37
NC_000019.8:g.60357206_60357209del	NCBI36
NG_007866.2:g.8707_8710del , LRG_432:g.8707_8710del
NG_011829.2:g.213_216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+4_549+7del MANE Select	ENSP00000341838.5:n.549+4_549+7del
ENST00000665070.1:c.582+4_582+7del	ENSP00000499482.1:n.582+4_582+7del
ENST00000344887.9:c.549+4_549+7del	ENSP00000341838.5:n.549+4_549+7del
ENST00000585806.5:n.548+4_548+7del
ENST00000588882.1:c.474+4_474+7del	ENSP00000466729.1:n.474+4_474+7del
ENST00000589864.1:n.377+4_377+7del
NM_000363.4:c.549+4_549+7del , LRG_432t1:c.549+4_549+7del	NP_000354.4:n.549+4_549+7del
NM_000363.5:c.549+4_549+7del MANE Select	NP_000354.4:n.549+4_549+7del