Canonical Allele Identifier: CA407441087

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55154794-C-G
• MyVariant Identifiers: chr19:g.55666162C>G (hg19) ; chr19:g.55154794C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154794C>G , CM000681.2:g.55154794C>G	GRCh38
NC_000019.9:g.55666162C>G , CM000681.1:g.55666162C>G	GRCh37
NC_000019.8:g.60357974C>G	NCBI36
NG_007866.2:g.7939G>C , LRG_432:g.7939G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.319G>C MANE Select	ENSP00000341838.5:p.Val107Leu
ENST00000665070.1:c.319G>C	ENSP00000499482.1:p.Val107Leu
ENST00000344887.9:c.319G>C	ENSP00000341838.5:p.Val107Leu
ENST00000585806.5:n.318G>C
ENST00000586669.5:n.327G>C
ENST00000587176.5:n.503G>C
ENST00000587871.1:c.938G>C
ENST00000588882.1:c.244G>C	ENSP00000466729.1:p.Val82Leu
ENST00000590463.1:n.491G>C
NM_000363.4:c.319G>C , LRG_432t1:c.319G>C	NP_000354.4:p.Val107Leu
NM_000363.5:c.319G>C MANE Select	NP_000354.4:p.Val107Leu