Canonical Allele Identifier: CA2343272645
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151898T= , CM000681.2:g.55151898T= GRCh38
NC_000019.9:g.55663266T= , CM000681.1:g.55663266T= GRCh37
NC_000019.8:g.60355078T= NCBI36
NG_007866.2:g.10835A= , LRG_432:g.10835A=
NG_011829.2:g.2341A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.569A= MANE Select ENSP00000341838.5:p.Asp190=
ENST00000665070.1:c.602A= ENSP00000499482.1:p.Asp201=
ENST00000344887.9:c.569A= ENSP00000341838.5:p.Asp190=
ENST00000585806.5:n.568A=
ENST00000588882.1:c.494A= ENSP00000466729.1:p.Asp165=
ENST00000589864.1:n.397A=
NM_000363.4:c.569A= , LRG_432t1:c.569A= NP_000354.4:p.Asp190=
NM_000363.5:c.569A= MANE Select NP_000354.4:p.Asp190=