Canonical Allele Identifier: CA407441141
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154809C>G , CM000681.2:g.55154809C>G GRCh38
NC_000019.9:g.55666177C>G , CM000681.1:g.55666177C>G GRCh37
NC_000019.8:g.60357989C>G NCBI36
NG_007866.2:g.7924G>C , LRG_432:g.7924G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.304G>C MANE Select ENSP00000341838.5:p.Ala102Pro
ENST00000665070.1:c.304G>C ENSP00000499482.1:p.Ala102Pro
ENST00000344887.9:c.304G>C ENSP00000341838.5:p.Ala102Pro
ENST00000585806.5:n.303G>C
ENST00000586669.5:n.312G>C
ENST00000587176.5:n.488G>C
ENST00000587871.1:c.923G>C
ENST00000588882.1:c.229G>C ENSP00000466729.1:p.Ala77Pro
ENST00000590463.1:n.476G>C
NM_000363.4:c.304G>C , LRG_432t1:c.304G>C NP_000354.4:p.Ala102Pro
NM_000363.5:c.304G>C MANE Select NP_000354.4:p.Ala102Pro