Canonical Allele Identifier: CA2587243752
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154640T>G , CM000681.2:g.55154640T>G GRCh38
NC_000019.9:g.55666008T>G , CM000681.1:g.55666008T>G GRCh37
NC_000019.8:g.60357820T>G NCBI36
NG_007866.2:g.8093A>C , LRG_432:g.8093A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.372+101A>C MANE Select ENSP00000341838.5:n.372+101A>C
ENST00000665070.1:c.405+68A>C ENSP00000499482.1:n.405+68A>C
ENST00000344887.9:c.372+101A>C ENSP00000341838.5:n.372+101A>C
ENST00000585806.5:n.371+101A>C
ENST00000586669.5:n.380+101A>C
ENST00000587176.5:n.657A>C
ENST00000588882.1:c.297+101A>C ENSP00000466729.1:n.297+101A>C
NM_000363.4:c.372+101A>C , LRG_432t1:c.372+101A>C NP_000354.4:n.372+101A>C
NM_000363.5:c.372+101A>C MANE Select NP_000354.4:n.372+101A>C