Canonical Allele Identifier: CA407441953

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55156302-G-T
• MyVariant Identifiers: chr19:g.55667670G>T (hg19) ; chr19:g.55156302G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156302G>T , CM000681.2:g.55156302G>T	GRCh38
NC_000019.9:g.55667670G>T , CM000681.1:g.55667670G>T	GRCh37
NC_000019.8:g.60359482G>T	NCBI36
NG_007866.2:g.6431C>A , LRG_432:g.6431C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.181C>A MANE Select	ENSP00000341838.5:p.Leu61Met
ENST00000665070.1:c.181C>A	ENSP00000499482.1:p.Leu61Met
ENST00000344887.9:c.181C>A	ENSP00000341838.5:p.Leu61Met
ENST00000585806.5:n.180C>A
ENST00000586669.5:n.189C>A
ENST00000586858.1:c.144C>A	ENSP00000465258.1:p.Ser48Arg
ENST00000587176.5:n.365C>A
ENST00000587871.1:c.800C>A
ENST00000588882.1:c.106C>A	ENSP00000466729.1:p.Leu36Met
ENST00000590463.1:n.353C>A
NM_000363.4:c.181C>A , LRG_432t1:c.181C>A	NP_000354.4:p.Leu61Met
NM_000363.5:c.181C>A MANE Select	NP_000354.4:p.Leu61Met