Canonical Allele Identifier: CA407441664

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55156206-G-T
• MyVariant Identifiers: chr19:g.55667574G>T (hg19) ; chr19:g.55156206G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156206G>T , CM000681.2:g.55156206G>T	GRCh38
NC_000019.9:g.55667574G>T , CM000681.1:g.55667574G>T	GRCh37
NC_000019.8:g.60359386G>T	NCBI36
NG_007866.2:g.6527C>A , LRG_432:g.6527C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.277C>A MANE Select	ENSP00000341838.5:p.Leu93Met
ENST00000665070.1:c.277C>A	ENSP00000499482.1:p.Leu93Met
ENST00000344887.9:c.277C>A	ENSP00000341838.5:p.Leu93Met
ENST00000585806.5:n.276C>A
ENST00000586669.5:n.285C>A
ENST00000587176.5:n.461C>A
ENST00000587871.1:c.896C>A
ENST00000588882.1:c.202C>A	ENSP00000466729.1:p.Leu68Met
ENST00000590463.1:n.449C>A
NM_000363.4:c.277C>A , LRG_432t1:c.277C>A	NP_000354.4:p.Leu93Met
NM_000363.5:c.277C>A MANE Select	NP_000354.4:p.Leu93Met