Canonical Allele Identifier: CA508989454

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55154156-C-T
• MyVariant Identifiers: chr19:g.55665524C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154156C>T , CM000681.2:g.55154156C>T	GRCh38
NC_000019.9:g.55665524C>T , CM000681.1:g.55665524C>T	GRCh37
NC_000019.8:g.60357336C>T	NCBI36
NG_007866.2:g.8577G>A , LRG_432:g.8577G>A
NG_011829.2:g.83G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.423G>A MANE Select	ENSP00000341838.5:p.Arg141=
ENST00000665070.1:c.456G>A	ENSP00000499482.1:p.Arg152=
ENST00000344887.9:c.423G>A	ENSP00000341838.5:p.Arg141=
ENST00000585806.5:n.422G>A
ENST00000586669.5:n.431G>A
ENST00000588882.1:c.348G>A	ENSP00000466729.1:p.Arg116=
ENST00000589864.1:n.251G>A
NM_000363.4:c.423G>A , LRG_432t1:c.423G>A	NP_000354.4:p.Arg141=
NM_000363.5:c.423G>A MANE Select	NP_000354.4:p.Arg141=