Canonical Allele Identifier: CA508989415

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665472G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154104G>A , CM000681.2:g.55154104G>A	GRCh38
NC_000019.9:g.55665472G>A , CM000681.1:g.55665472G>A	GRCh37
NC_000019.8:g.60357284G>A	NCBI36
NG_007866.2:g.8629C>T , LRG_432:g.8629C>T
NG_011829.2:g.135C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.475C>T MANE Select	ENSP00000341838.5:p.Leu159=
ENST00000665070.1:c.508C>T	ENSP00000499482.1:p.Leu170=
ENST00000344887.9:c.475C>T	ENSP00000341838.5:p.Leu159=
ENST00000585806.5:n.474C>T
ENST00000588882.1:c.400C>T	ENSP00000466729.1:p.Leu134=
ENST00000589864.1:n.303C>T
NM_000363.4:c.475C>T , LRG_432t1:c.475C>T	NP_000354.4:p.Leu159=
NM_000363.5:c.475C>T MANE Select	NP_000354.4:p.Leu159=