Canonical Allele Identifier: CA407441943

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667668C>T (hg19) ; chr19:g.55156300C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156300C>T , CM000681.2:g.55156300C>T	GRCh38
NC_000019.9:g.55667668C>T , CM000681.1:g.55667668C>T	GRCh37
NC_000019.8:g.60359480C>T	NCBI36
NG_007866.2:g.6433G>A , LRG_432:g.6433G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.183G>A MANE Select	ENSP00000341838.5:p.Leu61=
ENST00000665070.1:c.183G>A	ENSP00000499482.1:p.Leu61=
ENST00000344887.9:c.183G>A	ENSP00000341838.5:p.Leu61=
ENST00000585806.5:n.182G>A
ENST00000586669.5:n.191G>A
ENST00000586858.1:c.146G>A	ENSP00000465258.1:p.Trp49Ter
ENST00000587176.5:n.367G>A
ENST00000587871.1:c.802G>A
ENST00000588882.1:c.108G>A	ENSP00000466729.1:p.Leu36=
ENST00000590463.1:n.355G>A
NM_000363.4:c.183G>A , LRG_432t1:c.183G>A	NP_000354.4:p.Leu61=
NM_000363.5:c.183G>A MANE Select	NP_000354.4:p.Leu61=