Canonical Allele Identifier: CA407441956

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667671C>G (hg19) ; chr19:g.55156303C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156303C>G , CM000681.2:g.55156303C>G	GRCh38
NC_000019.9:g.55667671C>G , CM000681.1:g.55667671C>G	GRCh37
NC_000019.8:g.60359483C>G	NCBI36
NG_007866.2:g.6430G>C , LRG_432:g.6430G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.180G>C MANE Select	ENSP00000341838.5:p.Glu60Asp
ENST00000665070.1:c.180G>C	ENSP00000499482.1:p.Glu60Asp
ENST00000344887.9:c.180G>C	ENSP00000341838.5:p.Glu60Asp
ENST00000585806.5:n.179G>C
ENST00000586669.5:n.188G>C
ENST00000586858.1:c.143G>C	ENSP00000465258.1:p.Ser48Thr
ENST00000587176.5:n.364G>C
ENST00000587871.1:c.799G>C
ENST00000588882.1:c.105G>C	ENSP00000466729.1:p.Glu35Asp
ENST00000590463.1:n.352G>C
NM_000363.4:c.180G>C , LRG_432t1:c.180G>C	NP_000354.4:p.Glu60Asp
NM_000363.5:c.180G>C MANE Select	NP_000354.4:p.Glu60Asp