Canonical Allele Identifier: CA2343275951
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157589T= , CM000681.2:g.55157589T= GRCh38
NC_000019.9:g.55668957T= , CM000681.1:g.55668957T= GRCh37
NC_000019.8:g.60360769T= NCBI36
NG_007866.2:g.5144A= , LRG_432:g.5144A=
NG_032759.1:g.14134A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.1A= MANE Select ENSP00000341838.5:p.Met1=
ENST00000665070.1:c.1A= ENSP00000499482.1:p.Met1=
ENST00000344887.9:c.1A= ENSP00000341838.5:p.Met1=
ENST00000586446.1:n.144A=
ENST00000587176.5:n.185A=
ENST00000587871.1:c.621A=
ENST00000590463.1:n.128A=
NM_000363.4:c.1A= , LRG_432t1:c.1A= NP_000354.4:p.Met1=
NM_000363.5:c.1A= MANE Select NP_000354.4:p.Met1=