Canonical Allele Identifier: CA508989445
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665515C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154147C>T , CM000681.2:g.55154147C>T GRCh38
NC_000019.9:g.55665515C>T , CM000681.1:g.55665515C>T GRCh37
NC_000019.8:g.60357327C>T NCBI36
NG_007866.2:g.8586G>A , LRG_432:g.8586G>A
NG_011829.2:g.92G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.432G>A MANE Select ENSP00000341838.5:p.Leu144=
ENST00000665070.1:c.465G>A ENSP00000499482.1:p.Leu155=
ENST00000344887.9:c.432G>A ENSP00000341838.5:p.Leu144=
ENST00000585806.5:n.431G>A
ENST00000586669.5:n.440G>A
ENST00000588882.1:c.357G>A ENSP00000466729.1:p.Leu119=
ENST00000589864.1:n.260G>A
NM_000363.4:c.432G>A , LRG_432t1:c.432G>A NP_000354.4:p.Leu144=
NM_000363.5:c.432G>A MANE Select NP_000354.4:p.Leu144=
Search 100 bp 5'
Search 100 bp 3'