Canonical Allele Identifier: CA407440693

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55154177-G-T
• MyVariant Identifiers: chr19:g.55665545G>T (hg19) ; chr19:g.55154177G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154177G>T , CM000681.2:g.55154177G>T	GRCh38
NC_000019.9:g.55665545G>T , CM000681.1:g.55665545G>T	GRCh37
NC_000019.8:g.60357357G>T	NCBI36
NG_007866.2:g.8556C>A , LRG_432:g.8556C>A
NG_011829.2:g.62C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.402C>A MANE Select	ENSP00000341838.5:p.Asp134Glu
ENST00000665070.1:c.435C>A	ENSP00000499482.1:p.Asp145Glu
ENST00000344887.9:c.402C>A	ENSP00000341838.5:p.Asp134Glu
ENST00000585806.5:n.401C>A
ENST00000586669.5:n.410C>A
ENST00000588882.1:c.327C>A	ENSP00000466729.1:p.Asp109Glu
ENST00000589864.1:n.230C>A
NM_000363.4:c.402C>A , LRG_432t1:c.402C>A	NP_000354.4:p.Asp134Glu
NM_000363.5:c.402C>A MANE Select	NP_000354.4:p.Asp134Glu