Canonical Allele Identifier: CA2740096976

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 3009516
• ClinVar RCV Id: RCV003864627

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154835A>G , CM000681.2:g.55154835A>G	GRCh38
NC_000019.9:g.55666203A>G , CM000681.1:g.55666203A>G	GRCh37
NC_000019.8:g.60358015A>G	NCBI36
NG_007866.2:g.7898T>C , LRG_432:g.7898T>C

Transcript Alleles

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