Canonical Allele Identifier: CA407439402

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55151842-C-A
• MyVariant Identifiers: chr19:g.55663210C>A (hg19) ; chr19:g.55151842C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151842C>A , CM000681.2:g.55151842C>A	GRCh38
NC_000019.9:g.55663210C>A , CM000681.1:g.55663210C>A	GRCh37
NC_000019.8:g.60355022C>A	NCBI36
NG_007866.2:g.10891G>T , LRG_432:g.10891G>T
NG_011829.2:g.2397G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.625G>T MANE Select	ENSP00000341838.5:p.Glu209Ter
ENST00000665070.1:c.658G>T	ENSP00000499482.1:p.Glu220Ter
ENST00000344887.9:c.625G>T	ENSP00000341838.5:p.Glu209Ter
ENST00000585806.5:n.624G>T
ENST00000588882.1:c.550G>T	ENSP00000466729.1:p.Glu184Ter
ENST00000589864.1:n.453G>T
NM_000363.4:c.625G>T , LRG_432t1:c.625G>T	NP_000354.4:p.Glu209Ter
NM_000363.5:c.625G>T MANE Select	NP_000354.4:p.Glu209Ter