Canonical Allele Identifier: CA407440752

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665557C>A (hg19) ; chr19:g.55154189C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154189C>A , CM000681.2:g.55154189C>A	GRCh38
NC_000019.9:g.55665557C>A , CM000681.1:g.55665557C>A	GRCh37
NC_000019.8:g.60357369C>A	NCBI36
NG_007866.2:g.8544G>T , LRG_432:g.8544G>T
NG_011829.2:g.50G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.390G>T MANE Select	ENSP00000341838.5:p.Gln130His
ENST00000665070.1:c.423G>T	ENSP00000499482.1:p.Gln141His
ENST00000344887.9:c.390G>T	ENSP00000341838.5:p.Gln130His
ENST00000585806.5:n.389G>T
ENST00000586669.5:n.398G>T
ENST00000588882.1:c.315G>T	ENSP00000466729.1:p.Gln105His
ENST00000589864.1:n.218G>T
NM_000363.4:c.390G>T , LRG_432t1:c.390G>T	NP_000354.4:p.Gln130His
NM_000363.5:c.390G>T MANE Select	NP_000354.4:p.Gln130His