Canonical Allele Identifier: CA407441923

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 2798268
• ClinVar RCV Id: RCV003749272
• dbSNP Id: rs1286340820
• gnomAD v2: 19-55667664-G-A
• gnomAD v4: 19-55156296-G-A
• MyVariant Identifiers: chr19:g.55667664G>A (hg19) ; chr19:g.55156296G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156296G>A , CM000681.2:g.55156296G>A	GRCh38
NC_000019.9:g.55667664G>A , CM000681.1:g.55667664G>A	GRCh37
NC_000019.8:g.60359476G>A	NCBI36
NG_007866.2:g.6437C>T , LRG_432:g.6437C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.187C>T MANE Select	ENSP00000341838.5:p.Arg63Ter
ENST00000665070.1:c.187C>T	ENSP00000499482.1:p.Arg63Ter
ENST00000344887.9:c.187C>T	ENSP00000341838.5:p.Arg63Ter
ENST00000585806.5:n.186C>T
ENST00000586669.5:n.195C>T
ENST00000586858.1:c.150C>T	ENSP00000465258.1:p.Ser50=
ENST00000587176.5:n.371C>T
ENST00000587871.1:c.806C>T
ENST00000588882.1:c.112C>T	ENSP00000466729.1:p.Arg38Ter
ENST00000590463.1:n.359C>T
NM_000363.4:c.187C>T , LRG_432t1:c.187C>T	NP_000354.4:p.Arg63Ter
NM_000363.5:c.187C>T MANE Select	NP_000354.4:p.Arg63Ter