Canonical Allele Identifier: CA407440371

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 1918212
• ClinVar RCV Id: RCV002601846
• MyVariant Identifiers: chr19:g.55665466C>G (hg19) ; chr19:g.55154098C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154098C>G , CM000681.2:g.55154098C>G	GRCh38
NC_000019.9:g.55665466C>G , CM000681.1:g.55665466C>G	GRCh37
NC_000019.8:g.60357278C>G	NCBI36
NG_007866.2:g.8635G>C , LRG_432:g.8635G>C
NG_011829.2:g.141G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.481G>C MANE Select	ENSP00000341838.5:p.Ala161Pro
ENST00000665070.1:c.514G>C	ENSP00000499482.1:p.Ala172Pro
ENST00000344887.9:c.481G>C	ENSP00000341838.5:p.Ala161Pro
ENST00000585806.5:n.480G>C
ENST00000588882.1:c.406G>C	ENSP00000466729.1:p.Ala136Pro
ENST00000589864.1:n.309G>C
NM_000363.4:c.481G>C , LRG_432t1:c.481G>C	NP_000354.4:p.Ala161Pro
NM_000363.5:c.481G>C MANE Select	NP_000354.4:p.Ala161Pro