Canonical Allele Identifier: CA407440576

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55154155-G-A
• MyVariant Identifiers: chr19:g.55665523G>A (hg19) ; chr19:g.55154155G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154155G>A , CM000681.2:g.55154155G>A	GRCh38
NC_000019.9:g.55665523G>A , CM000681.1:g.55665523G>A	GRCh37
NC_000019.8:g.60357335G>A	NCBI36
NG_007866.2:g.8578C>T , LRG_432:g.8578C>T
NG_011829.2:g.84C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.424C>T MANE Select	ENSP00000341838.5:p.Pro142Ser
ENST00000665070.1:c.457C>T	ENSP00000499482.1:p.Pro153Ser
ENST00000344887.9:c.424C>T	ENSP00000341838.5:p.Pro142Ser
ENST00000585806.5:n.423C>T
ENST00000586669.5:n.432C>T
ENST00000588882.1:c.349C>T	ENSP00000466729.1:p.Pro117Ser
ENST00000589864.1:n.252C>T
NM_000363.4:c.424C>T , LRG_432t1:c.424C>T	NP_000354.4:p.Pro142Ser
NM_000363.5:c.424C>T MANE Select	NP_000354.4:p.Pro142Ser