Canonical Allele Identifier: CA407440714

Gene: TNNI3

Linked Data

• dbSNP Id: rs1599909285
• MyVariant Identifiers: chr19:g.55665549A>T (hg19) ; chr19:g.55154181A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154181A>T , CM000681.2:g.55154181A>T	GRCh38
NC_000019.9:g.55665549A>T , CM000681.1:g.55665549A>T	GRCh37
NC_000019.8:g.60357361A>T	NCBI36
NG_007866.2:g.8552T>A , LRG_432:g.8552T>A
NG_011829.2:g.58T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.398T>A MANE Select	ENSP00000341838.5:p.Phe133Tyr
ENST00000665070.1:c.431T>A	ENSP00000499482.1:p.Phe144Tyr
ENST00000344887.9:c.398T>A	ENSP00000341838.5:p.Phe133Tyr
ENST00000585806.5:n.397T>A
ENST00000586669.5:n.406T>A
ENST00000588882.1:c.323T>A	ENSP00000466729.1:p.Phe108Tyr
ENST00000589864.1:n.226T>A
NM_000363.4:c.398T>A , LRG_432t1:c.398T>A	NP_000354.4:p.Phe133Tyr
NM_000363.5:c.398T>A MANE Select	NP_000354.4:p.Phe133Tyr