Canonical Allele Identifier: CA407440935
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154752T>G , CM000681.2:g.55154752T>G GRCh38
NC_000019.9:g.55666120T>G , CM000681.1:g.55666120T>G GRCh37
NC_000019.8:g.60357932T>G NCBI36
NG_007866.2:g.7981A>C , LRG_432:g.7981A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.361A>C MANE Select ENSP00000341838.5:p.Asn121His
ENST00000665070.1:c.361A>C ENSP00000499482.1:p.Asn121His
ENST00000344887.9:c.361A>C ENSP00000341838.5:p.Asn121His
ENST00000585806.5:n.360A>C
ENST00000586669.5:n.369A>C
ENST00000587176.5:n.545A>C
ENST00000588882.1:c.286A>C ENSP00000466729.1:p.Asn96His
ENST00000590463.1:n.533A>C
NM_000363.4:c.361A>C , LRG_432t1:c.361A>C NP_000354.4:p.Asn121His
NM_000363.5:c.361A>C MANE Select NP_000354.4:p.Asn121His