Canonical Allele Identifier: CA407440357

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 2726864
• ClinVar RCV Id: RCV003587198
• MyVariant Identifiers: chr19:g.55665460C>G (hg19) ; chr19:g.55154092C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154092C>G , CM000681.2:g.55154092C>G	GRCh38
NC_000019.9:g.55665460C>G , CM000681.1:g.55665460C>G	GRCh37
NC_000019.8:g.60357272C>G	NCBI36
NG_007866.2:g.8641G>C , LRG_432:g.8641G>C
NG_011829.2:g.147G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.487G>C MANE Select	ENSP00000341838.5:p.Ala163Pro
ENST00000665070.1:c.520G>C	ENSP00000499482.1:p.Ala174Pro
ENST00000344887.9:c.487G>C	ENSP00000341838.5:p.Ala163Pro
ENST00000585806.5:n.486G>C
ENST00000588882.1:c.412G>C	ENSP00000466729.1:p.Ala138Pro
ENST00000589864.1:n.315G>C
NM_000363.4:c.487G>C , LRG_432t1:c.487G>C	NP_000354.4:p.Ala163Pro
NM_000363.5:c.487G>C MANE Select	NP_000354.4:p.Ala163Pro