Canonical Allele Identifier: CA407441089
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154795C>A , CM000681.2:g.55154795C>A GRCh38
NC_000019.9:g.55666163C>A , CM000681.1:g.55666163C>A GRCh37
NC_000019.8:g.60357975C>A NCBI36
NG_007866.2:g.7938G>T , LRG_432:g.7938G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.318G>T MANE Select ENSP00000341838.5:p.Lys106Asn
ENST00000665070.1:c.318G>T ENSP00000499482.1:p.Lys106Asn
ENST00000344887.9:c.318G>T ENSP00000341838.5:p.Lys106Asn
ENST00000585806.5:n.317G>T
ENST00000586669.5:n.326G>T
ENST00000587176.5:n.502G>T
ENST00000587871.1:c.937G>T
ENST00000588882.1:c.243G>T ENSP00000466729.1:p.Lys81Asn
ENST00000590463.1:n.490G>T
NM_000363.4:c.318G>T , LRG_432t1:c.318G>T NP_000354.4:p.Lys106Asn
NM_000363.5:c.318G>T MANE Select NP_000354.4:p.Lys106Asn