Canonical Allele Identifier: CA10577112
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 229335
ClinVar RCV Id: RCV000216343
dbSNP Id: rs876658026

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151843A>C , CM000681.2:g.55151843A>C GRCh38
NC_000019.9:g.55663211A>C , CM000681.1:g.55663211A>C GRCh37
NC_000019.8:g.60355023A>C NCBI36
NG_007866.2:g.10890T>G , LRG_432:g.10890T>G
NG_011829.2:g.2396T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.624T>G MANE Select ENSP00000341838.5:p.Phe208Leu
ENST00000665070.1:c.657T>G ENSP00000499482.1:p.Phe219Leu
ENST00000344887.9:c.624T>G ENSP00000341838.5:p.Phe208Leu
ENST00000585806.5:n.623T>G
ENST00000588882.1:c.549T>G ENSP00000466729.1:p.Phe183Leu
ENST00000589864.1:n.452T>G
NM_000363.4:c.624T>G , LRG_432t1:c.624T>G NP_000354.4:p.Phe208Leu
NM_000363.5:c.624T>G MANE Select NP_000354.4:p.Phe208Leu