Canonical Allele Identifier: CA508989353

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55663268T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151900T>A , CM000681.2:g.55151900T>A	GRCh38
NC_000019.9:g.55663268T>A , CM000681.1:g.55663268T>A	GRCh37
NC_000019.8:g.60355080T>A	NCBI36
NG_007866.2:g.10833A>T , LRG_432:g.10833A>T
NG_011829.2:g.2339A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.567A>T MANE Select	ENSP00000341838.5:p.Gly189=
ENST00000665070.1:c.600A>T	ENSP00000499482.1:p.Gly200=
ENST00000344887.9:c.567A>T	ENSP00000341838.5:p.Gly189=
ENST00000585806.5:n.566A>T
ENST00000588882.1:c.492A>T	ENSP00000466729.1:p.Gly164=
ENST00000589864.1:n.395A>T
NM_000363.4:c.567A>T , LRG_432t1:c.567A>T	NP_000354.4:p.Gly189=
NM_000363.5:c.567A>T MANE Select	NP_000354.4:p.Gly189=