Canonical Allele Identifier: CA2343275950
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157587C= , CM000681.2:g.55157587C= GRCh38
NC_000019.9:g.55668955C= , CM000681.1:g.55668955C= GRCh37
NC_000019.8:g.60360767C= NCBI36
NG_007866.2:g.5146G= , LRG_432:g.5146G=
NG_032759.1:g.14136G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.3G= MANE Select ENSP00000341838.5:p.Met1=
ENST00000665070.1:c.3G= ENSP00000499482.1:p.Met1=
ENST00000344887.9:c.3G= ENSP00000341838.5:p.Met1=
ENST00000586446.1:n.146G=
ENST00000587176.5:n.187G=
ENST00000587871.1:c.623G=
ENST00000590463.1:n.130G=
NM_000363.4:c.3G= , LRG_432t1:c.3G= NP_000354.4:p.Met1=
NM_000363.5:c.3G= MANE Select NP_000354.4:p.Met1=