Canonical Allele Identifier: CA407440433

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665485C>G (hg19) ; chr19:g.55154117C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154117C>G , CM000681.2:g.55154117C>G	GRCh38
NC_000019.9:g.55665485C>G , CM000681.1:g.55665485C>G	GRCh37
NC_000019.8:g.60357297C>G	NCBI36
NG_007866.2:g.8616G>C , LRG_432:g.8616G>C
NG_011829.2:g.122G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.462G>C MANE Select	ENSP00000341838.5:p.Met154Ile
ENST00000665070.1:c.495G>C	ENSP00000499482.1:p.Met165Ile
ENST00000344887.9:c.462G>C	ENSP00000341838.5:p.Met154Ile
ENST00000585806.5:n.461G>C
ENST00000586669.5:n.470G>C
ENST00000588882.1:c.387G>C	ENSP00000466729.1:p.Met129Ile
ENST00000589864.1:n.290G>C
NM_000363.4:c.462G>C , LRG_432t1:c.462G>C	NP_000354.4:p.Met154Ile
NM_000363.5:c.462G>C MANE Select	NP_000354.4:p.Met154Ile