Canonical Allele Identifier: CA407440455

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665491A>T (hg19) ; chr19:g.55154123A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154123A>T , CM000681.2:g.55154123A>T	GRCh38
NC_000019.9:g.55665491A>T , CM000681.1:g.55665491A>T	GRCh37
NC_000019.8:g.60357303A>T	NCBI36
NG_007866.2:g.8610T>A , LRG_432:g.8610T>A
NG_011829.2:g.116T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.456T>A MANE Select	ENSP00000341838.5:p.Asp152Glu
ENST00000665070.1:c.489T>A	ENSP00000499482.1:p.Asp163Glu
ENST00000344887.9:c.456T>A	ENSP00000341838.5:p.Asp152Glu
ENST00000585806.5:n.455T>A
ENST00000586669.5:n.464T>A
ENST00000588882.1:c.381T>A	ENSP00000466729.1:p.Asp127Glu
ENST00000589864.1:n.284T>A
NM_000363.4:c.456T>A , LRG_432t1:c.456T>A	NP_000354.4:p.Asp152Glu
NM_000363.5:c.456T>A MANE Select	NP_000354.4:p.Asp152Glu