Canonical Allele Identifier: CA407441931

Gene: TNNI3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.186G>A MANE Select	ENSP00000341838.5:p.Glu62=
ENST00000665070.1:c.186G>A	ENSP00000499482.1:p.Glu62=
ENST00000344887.9:c.186G>A	ENSP00000341838.5:p.Glu62=
ENST00000585806.5:n.185G>A
ENST00000586669.5:n.194G>A
ENST00000586858.1:c.149G>A	ENSP00000465258.1:p.Ser50Asn
ENST00000587176.5:n.370G>A
ENST00000587871.1:c.805G>A
ENST00000588882.1:c.111G>A	ENSP00000466729.1:p.Glu37=
ENST00000590463.1:n.358G>A
NM_000363.4:c.186G>A , LRG_432t1:c.186G>A	NP_000354.4:p.Glu62=
NM_000363.5:c.186G>A MANE Select	NP_000354.4:p.Glu62=