Canonical Allele Identifier: CA407441034

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55666147A>G (hg19) ; chr19:g.55154779A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154779A>G , CM000681.2:g.55154779A>G	GRCh38
NC_000019.9:g.55666147A>G , CM000681.1:g.55666147A>G	GRCh37
NC_000019.8:g.60357959A>G	NCBI36
NG_007866.2:g.7954T>C , LRG_432:g.7954T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.334T>C MANE Select	ENSP00000341838.5:p.Tyr112His
ENST00000665070.1:c.334T>C	ENSP00000499482.1:p.Tyr112His
ENST00000344887.9:c.334T>C	ENSP00000341838.5:p.Tyr112His
ENST00000585806.5:n.333T>C
ENST00000586669.5:n.342T>C
ENST00000587176.5:n.518T>C
ENST00000587871.1:c.953T>C
ENST00000588882.1:c.259T>C	ENSP00000466729.1:p.Tyr87His
ENST00000590463.1:n.506T>C
NM_000363.4:c.334T>C , LRG_432t1:c.334T>C	NP_000354.4:p.Tyr112His
NM_000363.5:c.334T>C MANE Select	NP_000354.4:p.Tyr112His