Canonical Allele Identifier: CA407440182

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665399T>A (hg19) ; chr19:g.55154031T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154031T>A , CM000681.2:g.55154031T>A	GRCh38
NC_000019.9:g.55665399T>A , CM000681.1:g.55665399T>A	GRCh37
NC_000019.8:g.60357211T>A	NCBI36
NG_007866.2:g.8702A>T , LRG_432:g.8702A>T
NG_011829.2:g.208A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.548A>T MANE Select	ENSP00000341838.5:p.Lys183Met
ENST00000665070.1:c.581A>T	ENSP00000499482.1:p.Lys194Met
ENST00000344887.9:c.548A>T	ENSP00000341838.5:p.Lys183Met
ENST00000585806.5:n.547A>T
ENST00000588882.1:c.473A>T	ENSP00000466729.1:p.Lys158Met
ENST00000589864.1:n.376A>T
NM_000363.4:c.548A>T , LRG_432t1:c.548A>T	NP_000354.4:p.Lys183Met
NM_000363.5:c.548A>T MANE Select	NP_000354.4:p.Lys183Met