Canonical Allele Identifier: CA407441947

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667669A>C (hg19) ; chr19:g.55156301A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156301A>C , CM000681.2:g.55156301A>C	GRCh38
NC_000019.9:g.55667669A>C , CM000681.1:g.55667669A>C	GRCh37
NC_000019.8:g.60359481A>C	NCBI36
NG_007866.2:g.6432T>G , LRG_432:g.6432T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.182T>G MANE Select	ENSP00000341838.5:p.Leu61Arg
ENST00000665070.1:c.182T>G	ENSP00000499482.1:p.Leu61Arg
ENST00000344887.9:c.182T>G	ENSP00000341838.5:p.Leu61Arg
ENST00000585806.5:n.181T>G
ENST00000586669.5:n.190T>G
ENST00000586858.1:c.145T>G	ENSP00000465258.1:p.Trp49Gly
ENST00000587176.5:n.366T>G
ENST00000587871.1:c.801T>G
ENST00000588882.1:c.107T>G	ENSP00000466729.1:p.Leu36Arg
ENST00000590463.1:n.354T>G
NM_000363.4:c.182T>G , LRG_432t1:c.182T>G	NP_000354.4:p.Leu61Arg
NM_000363.5:c.182T>G MANE Select	NP_000354.4:p.Leu61Arg