Canonical Allele Identifier: CA10583865

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 237689
• ClinVar RCV Id: RCV000226371 ; RCV000253395 ; RCV001668391
• dbSNP Id: rs878853955
• MyVariant Identifiers: chr19:g.55667678T>C (hg19) ; chr19:g.55156310T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156310T>C , CM000681.2:g.55156310T>C	GRCh38
NC_000019.9:g.55667678T>C , CM000681.1:g.55667678T>C	GRCh37
NC_000019.8:g.60359490T>C	NCBI36
NG_007866.2:g.6423A>G , LRG_432:g.6423A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.173A>G MANE Select	ENSP00000341838.5:p.Lys58Arg
ENST00000665070.1:c.173A>G	ENSP00000499482.1:p.Lys58Arg
ENST00000344887.9:c.173A>G	ENSP00000341838.5:p.Lys58Arg
ENST00000585806.5:n.172A>G
ENST00000586669.5:n.181A>G
ENST00000586858.1:c.136A>G	ENSP00000465258.1:p.Ser46Gly
ENST00000587176.5:n.357A>G
ENST00000587871.1:c.792A>G
ENST00000588882.1:c.98A>G	ENSP00000466729.1:p.Lys33Arg
ENST00000590463.1:n.345A>G
NM_000363.4:c.173A>G , LRG_432t1:c.173A>G	NP_000354.4:p.Lys58Arg
NM_000363.5:c.173A>G MANE Select	NP_000354.4:p.Lys58Arg