Canonical Allele Identifier: CA407441051

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55666152T>G (hg19) ; chr19:g.55154784T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154784T>G , CM000681.2:g.55154784T>G	GRCh38
NC_000019.9:g.55666152T>G , CM000681.1:g.55666152T>G	GRCh37
NC_000019.8:g.60357964T>G	NCBI36
NG_007866.2:g.7949A>C , LRG_432:g.7949A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.329A>C MANE Select	ENSP00000341838.5:p.Glu110Ala
ENST00000665070.1:c.329A>C	ENSP00000499482.1:p.Glu110Ala
ENST00000344887.9:c.329A>C	ENSP00000341838.5:p.Glu110Ala
ENST00000585806.5:n.328A>C
ENST00000586669.5:n.337A>C
ENST00000587176.5:n.513A>C
ENST00000587871.1:c.948A>C
ENST00000588882.1:c.254A>C	ENSP00000466729.1:p.Glu85Ala
ENST00000590463.1:n.501A>C
NM_000363.4:c.329A>C , LRG_432t1:c.329A>C	NP_000354.4:p.Glu110Ala
NM_000363.5:c.329A>C MANE Select	NP_000354.4:p.Glu110Ala