Canonical Allele Identifier: CA508989444

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 3071814
• ClinVar RCV Id: RCV004016308
• gnomAD v4: 19-55154146-G-T
• MyVariant Identifiers: chr19:g.55665514G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154146G>T , CM000681.2:g.55154146G>T	GRCh38
NC_000019.9:g.55665514G>T , CM000681.1:g.55665514G>T	GRCh37
NC_000019.8:g.60357326G>T	NCBI36
NG_007866.2:g.8587C>A , LRG_432:g.8587C>A
NG_011829.2:g.93C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.433C>A MANE Select	ENSP00000341838.5:p.Arg145=
ENST00000665070.1:c.466C>A	ENSP00000499482.1:p.Arg156=
ENST00000344887.9:c.433C>A	ENSP00000341838.5:p.Arg145=
ENST00000585806.5:n.432C>A
ENST00000586669.5:n.441C>A
ENST00000588882.1:c.358C>A	ENSP00000466729.1:p.Arg120=
ENST00000589864.1:n.261C>A
NM_000363.4:c.433C>A , LRG_432t1:c.433C>A	NP_000354.4:p.Arg145=
NM_000363.5:c.433C>A MANE Select	NP_000354.4:p.Arg145=