Canonical Allele Identifier: CA508989440

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665511T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154143T>G , CM000681.2:g.55154143T>G	GRCh38
NC_000019.9:g.55665511T>G , CM000681.1:g.55665511T>G	GRCh37
NC_000019.8:g.60357323T>G	NCBI36
NG_007866.2:g.8590A>C , LRG_432:g.8590A>C
NG_011829.2:g.96A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.436A>C MANE Select	ENSP00000341838.5:p.Arg146=
ENST00000665070.1:c.469A>C	ENSP00000499482.1:p.Arg157=
ENST00000344887.9:c.436A>C	ENSP00000341838.5:p.Arg146=
ENST00000585806.5:n.435A>C
ENST00000586669.5:n.444A>C
ENST00000588882.1:c.361A>C	ENSP00000466729.1:p.Arg121=
ENST00000589864.1:n.264A>C
NM_000363.4:c.436A>C , LRG_432t1:c.436A>C	NP_000354.4:p.Arg146=
NM_000363.5:c.436A>C MANE Select	NP_000354.4:p.Arg146=