Canonical Allele Identifier: CA407441932

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667666T>A (hg19) ; chr19:g.55156298T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156298T>A , CM000681.2:g.55156298T>A	GRCh38
NC_000019.9:g.55667666T>A , CM000681.1:g.55667666T>A	GRCh37
NC_000019.8:g.60359478T>A	NCBI36
NG_007866.2:g.6435A>T , LRG_432:g.6435A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.185A>T MANE Select	ENSP00000341838.5:p.Glu62Val
ENST00000665070.1:c.185A>T	ENSP00000499482.1:p.Glu62Val
ENST00000344887.9:c.185A>T	ENSP00000341838.5:p.Glu62Val
ENST00000585806.5:n.184A>T
ENST00000586669.5:n.193A>T
ENST00000586858.1:c.148A>T	ENSP00000465258.1:p.Ser50Cys
ENST00000587176.5:n.369A>T
ENST00000587871.1:c.804A>T
ENST00000588882.1:c.110A>T	ENSP00000466729.1:p.Glu37Val
ENST00000590463.1:n.357A>T
NM_000363.4:c.185A>T , LRG_432t1:c.185A>T	NP_000354.4:p.Glu62Val
NM_000363.5:c.185A>T MANE Select	NP_000354.4:p.Glu62Val