Canonical Allele Identifier: CA407443570

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55668956A>T (hg19) ; chr19:g.55157588A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55157588A>T , CM000681.2:g.55157588A>T	GRCh38
NC_000019.9:g.55668956A>T , CM000681.1:g.55668956A>T	GRCh37
NC_000019.8:g.60360768A>T	NCBI36
NG_007866.2:g.5145T>A , LRG_432:g.5145T>A
NG_032759.1:g.14135T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.2T>A MANE Select	ENSP00000341838.5:p.Met1Lys
ENST00000665070.1:c.2T>A	ENSP00000499482.1:p.Met1Lys
ENST00000344887.9:c.2T>A	ENSP00000341838.5:p.Met1Lys
ENST00000586446.1:n.145T>A
ENST00000587176.5:n.186T>A
ENST00000587871.1:c.622T>A
ENST00000590463.1:n.129T>A
NM_000363.4:c.2T>A , LRG_432t1:c.2T>A	NP_000354.4:p.Met1Lys
NM_000363.5:c.2T>A MANE Select	NP_000354.4:p.Met1Lys