Canonical Allele Identifier: CA645617750

Gene: TNNI3

Linked Data

• COSMIC: COSM41529

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154834G>T , CM000681.2:g.55154834G>T	GRCh38
NC_000019.9:g.55666202G>T , CM000681.1:g.55666202G>T	GRCh37
NC_000019.8:g.60358014G>T	NCBI36
NG_007866.2:g.7899C>A , LRG_432:g.7899C>A

Transcript Alleles

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