Canonical Allele Identifier: CA021245
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 137684
dbSNP Id: rs139150276

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156661G>T , CM000681.2:g.55156661G>T GRCh38
NC_000019.9:g.55668029G>T , CM000681.1:g.55668029G>T GRCh37
NC_000019.8:g.60359841G>T NCBI36
NG_007866.2:g.6072C>A , LRG_432:g.6072C>A
NG_032759.1:g.15062C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.109-17C>A MANE Select ENSP00000341838.5:n.109-17C>A
ENST00000665070.1:c.109-17C>A ENSP00000499482.1:n.109-17C>A
ENST00000344887.9:c.109-17C>A ENSP00000341838.5:n.109-17C>A
ENST00000586669.5:n.117-17C>A
ENST00000586858.1:c.17C>A ENSP00000465258.1:p.Ser6Tyr
ENST00000587176.5:n.293-17C>A
ENST00000587871.1:c.728-17C>A
ENST00000588882.1:c.17C>A ENSP00000466729.1:p.Ser6Tyr
ENST00000590463.1:n.281-17C>A
NM_000363.4:c.109-17C>A , LRG_432t1:c.109-17C>A NP_000354.4:n.109-17C>A
NM_000363.5:c.109-17C>A MANE Select NP_000354.4:n.109-17C>A