Canonical Allele Identifier: CA508989422

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665488G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154120G>A , CM000681.2:g.55154120G>A	GRCh38
NC_000019.9:g.55665488G>A , CM000681.1:g.55665488G>A	GRCh37
NC_000019.8:g.60357300G>A	NCBI36
NG_007866.2:g.8613C>T , LRG_432:g.8613C>T
NG_011829.2:g.119C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.459C>T MANE Select	ENSP00000341838.5:p.Ala153=
ENST00000665070.1:c.492C>T	ENSP00000499482.1:p.Ala164=
ENST00000344887.9:c.459C>T	ENSP00000341838.5:p.Ala153=
ENST00000585806.5:n.458C>T
ENST00000586669.5:n.467C>T
ENST00000588882.1:c.384C>T	ENSP00000466729.1:p.Ala128=
ENST00000589864.1:n.287C>T
NM_000363.4:c.459C>T , LRG_432t1:c.459C>T	NP_000354.4:p.Ala153=
NM_000363.5:c.459C>T MANE Select	NP_000354.4:p.Ala153=