Canonical Allele Identifier: CA407441928

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667665C>A (hg19) ; chr19:g.55156297C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156297C>A , CM000681.2:g.55156297C>A	GRCh38
NC_000019.9:g.55667665C>A , CM000681.1:g.55667665C>A	GRCh37
NC_000019.8:g.60359477C>A	NCBI36
NG_007866.2:g.6436G>T , LRG_432:g.6436G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.186G>T MANE Select	ENSP00000341838.5:p.Glu62Asp
ENST00000665070.1:c.186G>T	ENSP00000499482.1:p.Glu62Asp
ENST00000344887.9:c.186G>T	ENSP00000341838.5:p.Glu62Asp
ENST00000585806.5:n.185G>T
ENST00000586669.5:n.194G>T
ENST00000586858.1:c.149G>T	ENSP00000465258.1:p.Ser50Ile
ENST00000587176.5:n.370G>T
ENST00000587871.1:c.805G>T
ENST00000588882.1:c.111G>T	ENSP00000466729.1:p.Glu37Asp
ENST00000590463.1:n.358G>T
NM_000363.4:c.186G>T , LRG_432t1:c.186G>T	NP_000354.4:p.Glu62Asp
NM_000363.5:c.186G>T MANE Select	NP_000354.4:p.Glu62Asp