Canonical Allele Identifier: CA508989451
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665521G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154153G>T , CM000681.2:g.55154153G>T GRCh38
NC_000019.9:g.55665521G>T , CM000681.1:g.55665521G>T GRCh37
NC_000019.8:g.60357333G>T NCBI36
NG_007866.2:g.8580C>A , LRG_432:g.8580C>A
NG_011829.2:g.86C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.426C>A MANE Select ENSP00000341838.5:p.Pro142=
ENST00000665070.1:c.459C>A ENSP00000499482.1:p.Pro153=
ENST00000344887.9:c.426C>A ENSP00000341838.5:p.Pro142=
ENST00000585806.5:n.425C>A
ENST00000586669.5:n.434C>A
ENST00000588882.1:c.351C>A ENSP00000466729.1:p.Pro117=
ENST00000589864.1:n.254C>A
NM_000363.4:c.426C>A , LRG_432t1:c.426C>A NP_000354.4:p.Pro142=
NM_000363.5:c.426C>A MANE Select NP_000354.4:p.Pro142=
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