Canonical Allele Identifier: CA915953049
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 664137
ClinVar RCV Id: RCV000822162
dbSNP Id: rs1599909151
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154094del , CM000681.2:g.55154094del GRCh38
NC_000019.9:g.55665462del , CM000681.1:g.55665462del GRCh37
NC_000019.8:g.60357274del NCBI36
NG_007866.2:g.8641del , LRG_432:g.8641del
NG_011829.2:g.147del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.487del MANE Select ENSP00000341838.5:p.Ala163LeufsTer14
ENST00000665070.1:c.520del ENSP00000499482.1:p.Ala174LeufsTer14
ENST00000344887.9:c.487del ENSP00000341838.5:p.Ala163LeufsTer14
ENST00000585806.5:n.486del
ENST00000588882.1:c.412del ENSP00000466729.1:p.Ala138LeufsTer14
ENST00000589864.1:n.315del
NM_000363.4:c.487del , LRG_432t1:c.487del NP_000354.4:p.Ala163LeufsTer14
NM_000363.5:c.487del MANE Select NP_000354.4:p.Ala163LeufsTer14
Search 100 bp 5'
Search 100 bp 3'