Canonical Allele Identifier: CA407441925

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667664G>C (hg19) ; chr19:g.55156296G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156296G>C , CM000681.2:g.55156296G>C	GRCh38
NC_000019.9:g.55667664G>C , CM000681.1:g.55667664G>C	GRCh37
NC_000019.8:g.60359476G>C	NCBI36
NG_007866.2:g.6437C>G , LRG_432:g.6437C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.187C>G MANE Select	ENSP00000341838.5:p.Arg63Gly
ENST00000665070.1:c.187C>G	ENSP00000499482.1:p.Arg63Gly
ENST00000344887.9:c.187C>G	ENSP00000341838.5:p.Arg63Gly
ENST00000585806.5:n.186C>G
ENST00000586669.5:n.195C>G
ENST00000586858.1:c.150C>G	ENSP00000465258.1:p.Ser50Arg
ENST00000587176.5:n.371C>G
ENST00000587871.1:c.806C>G
ENST00000588882.1:c.112C>G	ENSP00000466729.1:p.Arg38Gly
ENST00000590463.1:n.359C>G
NM_000363.4:c.187C>G , LRG_432t1:c.187C>G	NP_000354.4:p.Arg63Gly
NM_000363.5:c.187C>G MANE Select	NP_000354.4:p.Arg63Gly