Canonical Allele Identifier: CA407441914

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667661C>T (hg19) ; chr19:g.55156293C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156293C>T , CM000681.2:g.55156293C>T	GRCh38
NC_000019.9:g.55667661C>T , CM000681.1:g.55667661C>T	GRCh37
NC_000019.8:g.60359473C>T	NCBI36
NG_007866.2:g.6440G>A , LRG_432:g.6440G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.190G>A MANE Select	ENSP00000341838.5:p.Glu64Lys
ENST00000665070.1:c.190G>A	ENSP00000499482.1:p.Glu64Lys
ENST00000344887.9:c.190G>A	ENSP00000341838.5:p.Glu64Lys
ENST00000585806.5:n.189G>A
ENST00000586669.5:n.198G>A
ENST00000586858.1:c.153G>A	ENSP00000465258.1:p.Glu51=
ENST00000587176.5:n.374G>A
ENST00000587871.1:c.809G>A
ENST00000588882.1:c.115G>A	ENSP00000466729.1:p.Glu39Lys
ENST00000590463.1:n.362G>A
NM_000363.4:c.190G>A , LRG_432t1:c.190G>A	NP_000354.4:p.Glu64Lys
NM_000363.5:c.190G>A MANE Select	NP_000354.4:p.Glu64Lys