Canonical Allele Identifier: CA508989434

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 1740684
• ClinVar RCV Id: RCV002328335
• dbSNP Id: rs1599909209
• MyVariant Identifiers: chr19:g.55665503C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154135C>T , CM000681.2:g.55154135C>T	GRCh38
NC_000019.9:g.55665503C>T , CM000681.1:g.55665503C>T	GRCh37
NC_000019.8:g.60357315C>T	NCBI36
NG_007866.2:g.8598G>A , LRG_432:g.8598G>A
NG_011829.2:g.104G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.444G>A MANE Select	ENSP00000341838.5:p.Arg148=
ENST00000665070.1:c.477G>A	ENSP00000499482.1:p.Arg159=
ENST00000344887.9:c.444G>A	ENSP00000341838.5:p.Arg148=
ENST00000585806.5:n.443G>A
ENST00000586669.5:n.452G>A
ENST00000588882.1:c.369G>A	ENSP00000466729.1:p.Arg123=
ENST00000589864.1:n.272G>A
NM_000363.4:c.444G>A , LRG_432t1:c.444G>A	NP_000354.4:p.Arg148=
NM_000363.5:c.444G>A MANE Select	NP_000354.4:p.Arg148=