Canonical Allele Identifier: CA508989447

Gene: TNNI3

Linked Data

• dbSNP Id: rs1599909239
• MyVariant Identifiers: chr19:g.55665518G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154150G>A , CM000681.2:g.55154150G>A	GRCh38
NC_000019.9:g.55665518G>A , CM000681.1:g.55665518G>A	GRCh37
NC_000019.8:g.60357330G>A	NCBI36
NG_007866.2:g.8583C>T , LRG_432:g.8583C>T
NG_011829.2:g.89C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.429C>T MANE Select	ENSP00000341838.5:p.Thr143=
ENST00000665070.1:c.462C>T	ENSP00000499482.1:p.Thr154=
ENST00000344887.9:c.429C>T	ENSP00000341838.5:p.Thr143=
ENST00000585806.5:n.428C>T
ENST00000586669.5:n.437C>T
ENST00000588882.1:c.354C>T	ENSP00000466729.1:p.Thr118=
ENST00000589864.1:n.257C>T
NM_000363.4:c.429C>T , LRG_432t1:c.429C>T	NP_000354.4:p.Thr143=
NM_000363.5:c.429C>T MANE Select	NP_000354.4:p.Thr143=