Canonical Allele Identifier: CA2343273733
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154068C= , CM000681.2:g.55154068C= GRCh38
NC_000019.9:g.55665436C= , CM000681.1:g.55665436C= GRCh37
NC_000019.8:g.60357248C= NCBI36
NG_007866.2:g.8665G= , LRG_432:g.8665G=
NG_011829.2:g.171G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.511G= MANE Select ENSP00000341838.5:p.Ala171=
ENST00000665070.1:c.544G= ENSP00000499482.1:p.Ala182=
ENST00000344887.9:c.511G= ENSP00000341838.5:p.Ala171=
ENST00000585806.5:n.510G=
ENST00000588882.1:c.436G= ENSP00000466729.1:p.Ala146=
ENST00000589864.1:n.339G=
NM_000363.4:c.511G= , LRG_432t1:c.511G= NP_000354.4:p.Ala171=
NM_000363.5:c.511G= MANE Select NP_000354.4:p.Ala171=