Canonical Allele Identifier: CA407442072

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55156323-G-T
• MyVariant Identifiers: chr19:g.55667691G>T (hg19) ; chr19:g.55156323G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156323G>T , CM000681.2:g.55156323G>T	GRCh38
NC_000019.9:g.55667691G>T , CM000681.1:g.55667691G>T	GRCh37
NC_000019.8:g.60359503G>T	NCBI36
NG_007866.2:g.6410C>A , LRG_432:g.6410C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.160C>A MANE Select	ENSP00000341838.5:p.Leu54Met
ENST00000665070.1:c.160C>A	ENSP00000499482.1:p.Leu54Met
ENST00000344887.9:c.160C>A	ENSP00000341838.5:p.Leu54Met
ENST00000585806.5:n.159C>A
ENST00000586669.5:n.168C>A
ENST00000586858.1:c.123C>A	ENSP00000465258.1:p.Cys41Ter
ENST00000587176.5:n.344C>A
ENST00000587871.1:c.779C>A
ENST00000588882.1:c.85C>A	ENSP00000466729.1:p.Leu29Met
ENST00000590463.1:n.332C>A
NM_000363.4:c.160C>A , LRG_432t1:c.160C>A	NP_000354.4:p.Leu54Met
NM_000363.5:c.160C>A MANE Select	NP_000354.4:p.Leu54Met