Canonical Allele Identifier: CA508989518

Gene: TNNI3

Linked Data

• dbSNP Id: rs1599909694
• MyVariant Identifiers: chr19:g.55666175G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154807G>T , CM000681.2:g.55154807G>T	GRCh38
NC_000019.9:g.55666175G>T , CM000681.1:g.55666175G>T	GRCh37
NC_000019.8:g.60357987G>T	NCBI36
NG_007866.2:g.7926C>A , LRG_432:g.7926C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.306C>A MANE Select	ENSP00000341838.5:p.Ala102=
ENST00000665070.1:c.306C>A	ENSP00000499482.1:p.Ala102=
ENST00000344887.9:c.306C>A	ENSP00000341838.5:p.Ala102=
ENST00000585806.5:n.305C>A
ENST00000586669.5:n.314C>A
ENST00000587176.5:n.490C>A
ENST00000587871.1:c.925C>A
ENST00000588882.1:c.231C>A	ENSP00000466729.1:p.Ala77=
ENST00000590463.1:n.478C>A
NM_000363.4:c.306C>A , LRG_432t1:c.306C>A	NP_000354.4:p.Ala102=
NM_000363.5:c.306C>A MANE Select	NP_000354.4:p.Ala102=