Canonical Allele Identifier: CA407440732

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665553T>C (hg19) ; chr19:g.55154185T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154185T>C , CM000681.2:g.55154185T>C	GRCh38
NC_000019.9:g.55665553T>C , CM000681.1:g.55665553T>C	GRCh37
NC_000019.8:g.60357365T>C	NCBI36
NG_007866.2:g.8548A>G , LRG_432:g.8548A>G
NG_011829.2:g.54A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.394A>G MANE Select	ENSP00000341838.5:p.Ile132Val
ENST00000665070.1:c.427A>G	ENSP00000499482.1:p.Ile143Val
ENST00000344887.9:c.394A>G	ENSP00000341838.5:p.Ile132Val
ENST00000585806.5:n.393A>G
ENST00000586669.5:n.402A>G
ENST00000588882.1:c.319A>G	ENSP00000466729.1:p.Ile107Val
ENST00000589864.1:n.222A>G
NM_000363.4:c.394A>G , LRG_432t1:c.394A>G	NP_000354.4:p.Ile132Val
NM_000363.5:c.394A>G MANE Select	NP_000354.4:p.Ile132Val