Canonical Allele Identifier: CA657447790

Gene: TNNI3

Linked Data

• dbSNP Id: rs1453799576
• COSMIC: COSN26079276
• MyVariant Identifiers: chr19:g.55665139T>A (hg19) ; chr19:g.55153771T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153771T>A , CM000681.2:g.55153771T>A	GRCh38
NC_000019.9:g.55665139T>A , CM000681.1:g.55665139T>A	GRCh37
NC_000019.8:g.60356951T>A	NCBI36
NG_007866.2:g.8962A>T , LRG_432:g.8962A>T
NG_011829.2:g.468A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+259A>T MANE Select	ENSP00000341838.5:n.549+259A>T
ENST00000665070.1:c.582+259A>T	ENSP00000499482.1:n.582+259A>T
ENST00000344887.9:c.549+259A>T	ENSP00000341838.5:n.549+259A>T
ENST00000585806.5:n.548+259A>T
ENST00000588882.1:c.474+259A>T	ENSP00000466729.1:n.474+259A>T
ENST00000589864.1:n.377+259A>T
NM_000363.4:c.549+259A>T , LRG_432t1:c.549+259A>T	NP_000354.4:n.549+259A>T
NM_000363.5:c.549+259A>T MANE Select	NP_000354.4:n.549+259A>T