Canonical Allele Identifier: CA407441966

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667673C>A (hg19) ; chr19:g.55156305C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156305C>A , CM000681.2:g.55156305C>A	GRCh38
NC_000019.9:g.55667673C>A , CM000681.1:g.55667673C>A	GRCh37
NC_000019.8:g.60359485C>A	NCBI36
NG_007866.2:g.6428G>T , LRG_432:g.6428G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.178G>T MANE Select	ENSP00000341838.5:p.Glu60Ter
ENST00000665070.1:c.178G>T	ENSP00000499482.1:p.Glu60Ter
ENST00000344887.9:c.178G>T	ENSP00000341838.5:p.Glu60Ter
ENST00000585806.5:n.177G>T
ENST00000586669.5:n.186G>T
ENST00000586858.1:c.141G>T	ENSP00000465258.1:p.Lys47Asn
ENST00000587176.5:n.362G>T
ENST00000587871.1:c.797G>T
ENST00000588882.1:c.103G>T	ENSP00000466729.1:p.Glu35Ter
ENST00000590463.1:n.350G>T
NM_000363.4:c.178G>T , LRG_432t1:c.178G>T	NP_000354.4:p.Glu60Ter
NM_000363.5:c.178G>T MANE Select	NP_000354.4:p.Glu60Ter