Canonical Allele Identifier: CA021791
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 12429
dbSNP Id: rs121917761

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154068C>T , CM000681.2:g.55154068C>T GRCh38
NC_000019.9:g.55665436C>T , CM000681.1:g.55665436C>T GRCh37
NC_000019.8:g.60357248C>T NCBI36
NG_007866.2:g.8665G>A , LRG_432:g.8665G>A
NG_011829.2:g.171G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.511G>A MANE Select ENSP00000341838.5:p.Ala171Thr
ENST00000665070.1:c.544G>A ENSP00000499482.1:p.Ala182Thr
ENST00000344887.9:c.511G>A ENSP00000341838.5:p.Ala171Thr
ENST00000585806.5:n.510G>A
ENST00000588882.1:c.436G>A ENSP00000466729.1:p.Ala146Thr
ENST00000589864.1:n.339G>A
NM_000363.4:c.511G>A , LRG_432t1:c.511G>A NP_000354.4:p.Ala171Thr
NM_000363.5:c.511G>A MANE Select NP_000354.4:p.Ala171Thr