Canonical Allele Identifier: CA2343272506
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151860C= , CM000681.2:g.55151860C= GRCh38
NC_000019.9:g.55663228C= , CM000681.1:g.55663228C= GRCh37
NC_000019.8:g.60355040C= NCBI36
NG_007866.2:g.10873G= , LRG_432:g.10873G=
NG_011829.2:g.2379G=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.607G= MANE Select ENSP00000341838.5:p.Gly203=
ENST00000665070.1:c.640G= ENSP00000499482.1:p.Gly214=
ENST00000344887.9:c.607G= ENSP00000341838.5:p.Gly203=
ENST00000585806.5:n.606G=
ENST00000588882.1:c.532G= ENSP00000466729.1:p.Gly178=
ENST00000589864.1:n.435G=
NM_000363.4:c.607G= , LRG_432t1:c.607G= NP_000354.4:p.Gly203=
NM_000363.5:c.607G= MANE Select NP_000354.4:p.Gly203=