Canonical Allele Identifier: CA2842832843
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154111dup , CM000681.2:g.55154111dup GRCh38
NC_000019.9:g.55665479dup , CM000681.1:g.55665479dup GRCh37
NC_000019.8:g.60357291dup NCBI36
NG_007866.2:g.8623dup , LRG_432:g.8623dup
NG_011829.2:g.129dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.469dup MANE Select ENSP00000341838.5:p.Ala157GlyfsTer8
ENST00000665070.1:c.502dup ENSP00000499482.1:p.Ala168GlyfsTer8
ENST00000344887.9:c.469dup ENSP00000341838.5:p.Ala157GlyfsTer8
ENST00000585806.5:n.468dup
ENST00000588882.1:c.394dup ENSP00000466729.1:p.Ala132GlyfsTer8
ENST00000589864.1:n.297dup
NM_000363.4:c.469dup , LRG_432t1:c.469dup NP_000354.4:p.Ala157GlyfsTer8
NM_000363.5:c.469dup MANE Select NP_000354.4:p.Ala157GlyfsTer8