Canonical Allele Identifier: CA407439470

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55663228C>A (hg19) ; chr19:g.55151860C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151860C>A , CM000681.2:g.55151860C>A	GRCh38
NC_000019.9:g.55663228C>A , CM000681.1:g.55663228C>A	GRCh37
NC_000019.8:g.60355040C>A	NCBI36
NG_007866.2:g.10873G>T , LRG_432:g.10873G>T
NG_011829.2:g.2379G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.607G>T MANE Select	ENSP00000341838.5:p.Gly203Cys
ENST00000665070.1:c.640G>T	ENSP00000499482.1:p.Gly214Cys
ENST00000344887.9:c.607G>T	ENSP00000341838.5:p.Gly203Cys
ENST00000585806.5:n.606G>T
ENST00000588882.1:c.532G>T	ENSP00000466729.1:p.Gly178Cys
ENST00000589864.1:n.435G>T
NM_000363.4:c.607G>T , LRG_432t1:c.607G>T	NP_000354.4:p.Gly203Cys
NM_000363.5:c.607G>T MANE Select	NP_000354.4:p.Gly203Cys