Canonical Allele Identifier: CA407440619

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665531A>G (hg19) ; chr19:g.55154163A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154163A>G , CM000681.2:g.55154163A>G	GRCh38
NC_000019.9:g.55665531A>G , CM000681.1:g.55665531A>G	GRCh37
NC_000019.8:g.60357343A>G	NCBI36
NG_007866.2:g.8570T>C , LRG_432:g.8570T>C
NG_011829.2:g.76T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.416T>C MANE Select	ENSP00000341838.5:p.Phe139Ser
ENST00000665070.1:c.449T>C	ENSP00000499482.1:p.Phe150Ser
ENST00000344887.9:c.416T>C	ENSP00000341838.5:p.Phe139Ser
ENST00000585806.5:n.415T>C
ENST00000586669.5:n.424T>C
ENST00000588882.1:c.341T>C	ENSP00000466729.1:p.Phe114Ser
ENST00000589864.1:n.244T>C
NM_000363.4:c.416T>C , LRG_432t1:c.416T>C	NP_000354.4:p.Phe139Ser
NM_000363.5:c.416T>C MANE Select	NP_000354.4:p.Phe139Ser