Canonical Allele Identifier: CA407441681

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667582A>G (hg19) ; chr19:g.55156214A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156214A>G , CM000681.2:g.55156214A>G	GRCh38
NC_000019.9:g.55667582A>G , CM000681.1:g.55667582A>G	GRCh37
NC_000019.8:g.60359394A>G	NCBI36
NG_007866.2:g.6519T>C , LRG_432:g.6519T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.269T>C MANE Select	ENSP00000341838.5:p.Phe90Ser
ENST00000665070.1:c.269T>C	ENSP00000499482.1:p.Phe90Ser
ENST00000344887.9:c.269T>C	ENSP00000341838.5:p.Phe90Ser
ENST00000585806.5:n.268T>C
ENST00000586669.5:n.277T>C
ENST00000587176.5:n.453T>C
ENST00000587871.1:c.888T>C
ENST00000588882.1:c.194T>C	ENSP00000466729.1:p.Phe65Ser
ENST00000590463.1:n.441T>C
NM_000363.4:c.269T>C , LRG_432t1:c.269T>C	NP_000354.4:p.Phe90Ser
NM_000363.5:c.269T>C MANE Select	NP_000354.4:p.Phe90Ser