Canonical Allele Identifier: CA2695229163
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154836G>A , CM000681.2:g.55154836G>A GRCh38
NC_000019.9:g.55666204G>A , CM000681.1:g.55666204G>A GRCh37
NC_000019.8:g.60358016G>A NCBI36
NG_007866.2:g.7897C>T , LRG_432:g.7897C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.283-6C>T MANE Select ENSP00000341838.5:n.283-6C>T
ENST00000665070.1:c.283-6C>T ENSP00000499482.1:n.283-6C>T
ENST00000344887.9:c.283-6C>T ENSP00000341838.5:n.283-6C>T
ENST00000585806.5:n.282-6C>T
ENST00000586669.5:n.291-6C>T
ENST00000587176.5:n.467-6C>T
ENST00000587871.1:c.902-6C>T
ENST00000588882.1:c.208-6C>T ENSP00000466729.1:n.208-6C>T
ENST00000590463.1:n.455-6C>T
NM_000363.4:c.283-6C>T , LRG_432t1:c.283-6C>T NP_000354.4:n.283-6C>T
NM_000363.5:c.283-6C>T MANE Select NP_000354.4:n.283-6C>T