Canonical Allele Identifier: CA407440896

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55666108C>A (hg19) ; chr19:g.55154740C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154740C>A , CM000681.2:g.55154740C>A	GRCh38
NC_000019.9:g.55666108C>A , CM000681.1:g.55666108C>A	GRCh37
NC_000019.8:g.60357920C>A	NCBI36
NG_007866.2:g.7993G>T , LRG_432:g.7993G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.372+1G>T MANE Select	ENSP00000341838.5:n.372+1G>T
ENST00000665070.1:c.373G>T	ENSP00000499482.1:p.Val125Leu
ENST00000344887.9:c.372+1G>T	ENSP00000341838.5:n.372+1G>T
ENST00000585806.5:n.371+1G>T
ENST00000586669.5:n.380+1G>T
ENST00000587176.5:n.557G>T
ENST00000588882.1:c.297+1G>T	ENSP00000466729.1:n.297+1G>T
NM_000363.4:c.372+1G>T , LRG_432t1:c.372+1G>T	NP_000354.4:n.372+1G>T
NM_000363.5:c.372+1G>T MANE Select	NP_000354.4:n.372+1G>T