Canonical Allele Identifier: CA407440687

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665544G>C (hg19) ; chr19:g.55154176G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154176G>C , CM000681.2:g.55154176G>C	GRCh38
NC_000019.9:g.55665544G>C , CM000681.1:g.55665544G>C	GRCh37
NC_000019.8:g.60357356G>C	NCBI36
NG_007866.2:g.8557C>G , LRG_432:g.8557C>G
NG_011829.2:g.63C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.403C>G MANE Select	ENSP00000341838.5:p.Leu135Val
ENST00000665070.1:c.436C>G	ENSP00000499482.1:p.Leu146Val
ENST00000344887.9:c.403C>G	ENSP00000341838.5:p.Leu135Val
ENST00000585806.5:n.402C>G
ENST00000586669.5:n.411C>G
ENST00000588882.1:c.328C>G	ENSP00000466729.1:p.Leu110Val
ENST00000589864.1:n.231C>G
NM_000363.4:c.403C>G , LRG_432t1:c.403C>G	NP_000354.4:p.Leu135Val
NM_000363.5:c.403C>G MANE Select	NP_000354.4:p.Leu135Val