Canonical Allele Identifier: CA407442044

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667687T>A (hg19) ; chr19:g.55156319T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156319T>A , CM000681.2:g.55156319T>A	GRCh38
NC_000019.9:g.55667687T>A , CM000681.1:g.55667687T>A	GRCh37
NC_000019.8:g.60359499T>A	NCBI36
NG_007866.2:g.6414A>T , LRG_432:g.6414A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.164A>T MANE Select	ENSP00000341838.5:p.Gln55Leu
ENST00000665070.1:c.164A>T	ENSP00000499482.1:p.Gln55Leu
ENST00000344887.9:c.164A>T	ENSP00000341838.5:p.Gln55Leu
ENST00000585806.5:n.163A>T
ENST00000586669.5:n.172A>T
ENST00000586858.1:c.127A>T	ENSP00000465258.1:p.Arg43Ter
ENST00000587176.5:n.348A>T
ENST00000587871.1:c.783A>T
ENST00000588882.1:c.89A>T	ENSP00000466729.1:p.Gln30Leu
ENST00000590463.1:n.336A>T
NM_000363.4:c.164A>T , LRG_432t1:c.164A>T	NP_000354.4:p.Gln55Leu
NM_000363.5:c.164A>T MANE Select	NP_000354.4:p.Gln55Leu