Canonical Allele Identifier: CA407440303

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 1994254
• ClinVar RCV Id: RCV002806724
• MyVariant Identifiers: chr19:g.55665438C>G (hg19) ; chr19:g.55154070C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154070C>G , CM000681.2:g.55154070C>G	GRCh38
NC_000019.9:g.55665438C>G , CM000681.1:g.55665438C>G	GRCh37
NC_000019.8:g.60357250C>G	NCBI36
NG_007866.2:g.8663G>C , LRG_432:g.8663G>C
NG_011829.2:g.169G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.509G>C MANE Select	ENSP00000341838.5:p.Arg170Pro
ENST00000665070.1:c.542G>C	ENSP00000499482.1:p.Arg181Pro
ENST00000344887.9:c.509G>C	ENSP00000341838.5:p.Arg170Pro
ENST00000585806.5:n.508G>C
ENST00000588882.1:c.434G>C	ENSP00000466729.1:p.Arg145Pro
ENST00000589864.1:n.337G>C
NM_000363.4:c.509G>C , LRG_432t1:c.509G>C	NP_000354.4:p.Arg170Pro
NM_000363.5:c.509G>C MANE Select	NP_000354.4:p.Arg170Pro