Canonical Allele Identifier: CA407442056

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667688G>C (hg19) ; chr19:g.55156320G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156320G>C , CM000681.2:g.55156320G>C	GRCh38
NC_000019.9:g.55667688G>C , CM000681.1:g.55667688G>C	GRCh37
NC_000019.8:g.60359500G>C	NCBI36
NG_007866.2:g.6413C>G , LRG_432:g.6413C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.163C>G MANE Select	ENSP00000341838.5:p.Gln55Glu
ENST00000665070.1:c.163C>G	ENSP00000499482.1:p.Gln55Glu
ENST00000344887.9:c.163C>G	ENSP00000341838.5:p.Gln55Glu
ENST00000585806.5:n.162C>G
ENST00000586669.5:n.171C>G
ENST00000586858.1:c.126C>G	ENSP00000465258.1:p.Cys42Trp
ENST00000587176.5:n.347C>G
ENST00000587871.1:c.782C>G
ENST00000588882.1:c.88C>G	ENSP00000466729.1:p.Gln30Glu
ENST00000590463.1:n.335C>G
NM_000363.4:c.163C>G , LRG_432t1:c.163C>G	NP_000354.4:p.Gln55Glu
NM_000363.5:c.163C>G MANE Select	NP_000354.4:p.Gln55Glu