Canonical Allele Identifier: CA407441919

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667663C>A (hg19) ; chr19:g.55156295C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156295C>A , CM000681.2:g.55156295C>A	GRCh38
NC_000019.9:g.55667663C>A , CM000681.1:g.55667663C>A	GRCh37
NC_000019.8:g.60359475C>A	NCBI36
NG_007866.2:g.6438G>T , LRG_432:g.6438G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.188G>T MANE Select	ENSP00000341838.5:p.Arg63Leu
ENST00000665070.1:c.188G>T	ENSP00000499482.1:p.Arg63Leu
ENST00000344887.9:c.188G>T	ENSP00000341838.5:p.Arg63Leu
ENST00000585806.5:n.187G>T
ENST00000586669.5:n.196G>T
ENST00000586858.1:c.151G>T	ENSP00000465258.1:p.Glu51Ter
ENST00000587176.5:n.372G>T
ENST00000587871.1:c.807G>T
ENST00000588882.1:c.113G>T	ENSP00000466729.1:p.Arg38Leu
ENST00000590463.1:n.360G>T
NM_000363.4:c.188G>T , LRG_432t1:c.188G>T	NP_000354.4:p.Arg63Leu
NM_000363.5:c.188G>T MANE Select	NP_000354.4:p.Arg63Leu