Canonical Allele Identifier: CA407440380

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665469C>T (hg19) ; chr19:g.55154101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154101C>T , CM000681.2:g.55154101C>T	GRCh38
NC_000019.9:g.55665469C>T , CM000681.1:g.55665469C>T	GRCh37
NC_000019.8:g.60357281C>T	NCBI36
NG_007866.2:g.8632G>A , LRG_432:g.8632G>A
NG_011829.2:g.138G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.478G>A MANE Select	ENSP00000341838.5:p.Gly160Arg
ENST00000665070.1:c.511G>A	ENSP00000499482.1:p.Gly171Arg
ENST00000344887.9:c.478G>A	ENSP00000341838.5:p.Gly160Arg
ENST00000585806.5:n.477G>A
ENST00000588882.1:c.403G>A	ENSP00000466729.1:p.Gly135Arg
ENST00000589864.1:n.306G>A
NM_000363.4:c.478G>A , LRG_432t1:c.478G>A	NP_000354.4:p.Gly160Arg
NM_000363.5:c.478G>A MANE Select	NP_000354.4:p.Gly160Arg