Canonical Allele Identifier: CA021698

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 181582
• ClinVar RCV Id: RCV000159225
• dbSNP Id: rs730881073
• MyVariant Identifiers: chr19:g.55665489G>T (hg19) ; chr19:g.55154121G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154121G>T , CM000681.2:g.55154121G>T	GRCh38
NC_000019.9:g.55665489G>T , CM000681.1:g.55665489G>T	GRCh37
NC_000019.8:g.60357301G>T	NCBI36
NG_007866.2:g.8612C>A , LRG_432:g.8612C>A
NG_011829.2:g.118C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.458C>A MANE Select	ENSP00000341838.5:p.Ala153Asp
ENST00000665070.1:c.491C>A	ENSP00000499482.1:p.Ala164Asp
ENST00000344887.9:c.458C>A	ENSP00000341838.5:p.Ala153Asp
ENST00000585806.5:n.457C>A
ENST00000586669.5:n.466C>A
ENST00000588882.1:c.383C>A	ENSP00000466729.1:p.Ala128Asp
ENST00000589864.1:n.286C>A
NM_000363.4:c.458C>A , LRG_432t1:c.458C>A	NP_000354.4:p.Ala153Asp
NM_000363.5:c.458C>A MANE Select	NP_000354.4:p.Ala153Asp