Canonical Allele Identifier: CA2343273885
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs1266387013

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154355C>A , CM000681.2:g.55154355C>A GRCh38
NC_000019.9:g.55665723C>A , CM000681.1:g.55665723C>A GRCh37
NC_000019.8:g.60357535C>A NCBI36
NG_007866.2:g.8378G>T , LRG_432:g.8378G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.373-149G>T MANE Select ENSP00000341838.5:n.373-149G>T
ENST00000665070.1:c.406-149G>T ENSP00000499482.1:n.406-149G>T
ENST00000344887.9:c.373-149G>T ENSP00000341838.5:n.373-149G>T
ENST00000585806.5:n.372-149G>T
ENST00000586669.5:n.381-149G>T
ENST00000587176.5:n.942G>T
ENST00000588882.1:c.298-149G>T ENSP00000466729.1:n.298-149G>T
ENST00000589864.1:n.52G>T
NM_000363.4:c.373-149G>T , LRG_432t1:c.373-149G>T NP_000354.4:n.373-149G>T
NM_000363.5:c.373-149G>T MANE Select NP_000354.4:n.373-149G>T