Canonical Allele Identifier: CA407440462

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665493C>A (hg19) ; chr19:g.55154125C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154125C>A , CM000681.2:g.55154125C>A	GRCh38
NC_000019.9:g.55665493C>A , CM000681.1:g.55665493C>A	GRCh37
NC_000019.8:g.60357305C>A	NCBI36
NG_007866.2:g.8608G>T , LRG_432:g.8608G>T
NG_011829.2:g.114G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.454G>T MANE Select	ENSP00000341838.5:p.Asp152Tyr
ENST00000665070.1:c.487G>T	ENSP00000499482.1:p.Asp163Tyr
ENST00000344887.9:c.454G>T	ENSP00000341838.5:p.Asp152Tyr
ENST00000585806.5:n.453G>T
ENST00000586669.5:n.462G>T
ENST00000588882.1:c.379G>T	ENSP00000466729.1:p.Asp127Tyr
ENST00000589864.1:n.282G>T
NM_000363.4:c.454G>T , LRG_432t1:c.454G>T	NP_000354.4:p.Asp152Tyr
NM_000363.5:c.454G>T MANE Select	NP_000354.4:p.Asp152Tyr