Canonical Allele Identifier: CA407439622

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55663262C>G (hg19) ; chr19:g.55151894C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151894C>G , CM000681.2:g.55151894C>G	GRCh38
NC_000019.9:g.55663262C>G , CM000681.1:g.55663262C>G	GRCh37
NC_000019.8:g.60355074C>G	NCBI36
NG_007866.2:g.10839G>C , LRG_432:g.10839G>C
NG_011829.2:g.2345G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.573G>C MANE Select	ENSP00000341838.5:p.Trp191Cys
ENST00000665070.1:c.606G>C	ENSP00000499482.1:p.Trp202Cys
ENST00000344887.9:c.573G>C	ENSP00000341838.5:p.Trp191Cys
ENST00000585806.5:n.572G>C
ENST00000588882.1:c.498G>C	ENSP00000466729.1:p.Trp166Cys
ENST00000589864.1:n.401G>C
NM_000363.4:c.573G>C , LRG_432t1:c.573G>C	NP_000354.4:p.Trp191Cys
NM_000363.5:c.573G>C MANE Select	NP_000354.4:p.Trp191Cys