Canonical Allele Identifier: CA2576892663
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154727C>T , CM000681.2:g.55154727C>T GRCh38
NC_000019.9:g.55666095C>T , CM000681.1:g.55666095C>T GRCh37
NC_000019.8:g.60357907C>T NCBI36
NG_007866.2:g.8006G>A , LRG_432:g.8006G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.372+14G>A MANE Select ENSP00000341838.5:n.372+14G>A
ENST00000665070.1:c.386G>A ENSP00000499482.1:p.Gly129Asp
ENST00000344887.9:c.372+14G>A ENSP00000341838.5:n.372+14G>A
ENST00000585806.5:n.371+14G>A
ENST00000586669.5:n.380+14G>A
ENST00000587176.5:n.570G>A
ENST00000588882.1:c.297+14G>A ENSP00000466729.1:n.297+14G>A
NM_000363.4:c.372+14G>A , LRG_432t1:c.372+14G>A NP_000354.4:n.372+14G>A
NM_000363.5:c.372+14G>A MANE Select NP_000354.4:n.372+14G>A