Canonical Allele Identifier: CA407439639

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55663266T>A (hg19) ; chr19:g.55151898T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151898T>A , CM000681.2:g.55151898T>A	GRCh38
NC_000019.9:g.55663266T>A , CM000681.1:g.55663266T>A	GRCh37
NC_000019.8:g.60355078T>A	NCBI36
NG_007866.2:g.10835A>T , LRG_432:g.10835A>T
NG_011829.2:g.2341A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.569A>T MANE Select	ENSP00000341838.5:p.Asp190Val
ENST00000665070.1:c.602A>T	ENSP00000499482.1:p.Asp201Val
ENST00000344887.9:c.569A>T	ENSP00000341838.5:p.Asp190Val
ENST00000585806.5:n.568A>T
ENST00000588882.1:c.494A>T	ENSP00000466729.1:p.Asp165Val
ENST00000589864.1:n.397A>T
NM_000363.4:c.569A>T , LRG_432t1:c.569A>T	NP_000354.4:p.Asp190Val
NM_000363.5:c.569A>T MANE Select	NP_000354.4:p.Asp190Val