Canonical Allele Identifier: CA021648

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154148A>T , CM000681.2:g.55154148A>T	GRCh38
NC_000019.9:g.55665516A>T , CM000681.1:g.55665516A>T	GRCh37
NC_000019.8:g.60357328A>T	NCBI36
NG_007866.2:g.8585T>A , LRG_432:g.8585T>A
NG_011829.2:g.91T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000363.5:c.431T>A MANE Select	NP_000354.4:p.Leu144Gln
ENST00000344887.10:c.431T>A MANE Select	ENSP00000341838.5:p.Leu144Gln
NM_000363.4:c.431T>A , LRG_432t1:c.431T>A	NP_000354.4:p.Leu144Gln
ENST00000344887.9:c.431T>A	ENSP00000341838.5:p.Leu144Gln
ENST00000585806.5:n.430T>A
ENST00000586669.5:n.439T>A
ENST00000588882.1:c.356T>A	ENSP00000466729.1:p.Leu119Gln
ENST00000589864.1:n.259T>A
ENST00000665070.1:c.464T>A	ENSP00000499482.1:p.Leu155Gln