Canonical Allele Identifier: CA407440252

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665415T>A (hg19) ; chr19:g.55154047T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154047T>A , CM000681.2:g.55154047T>A	GRCh38
NC_000019.9:g.55665415T>A , CM000681.1:g.55665415T>A	GRCh37
NC_000019.8:g.60357227T>A	NCBI36
NG_007866.2:g.8686A>T , LRG_432:g.8686A>T
NG_011829.2:g.192A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.532A>T MANE Select	ENSP00000341838.5:p.Lys178Ter
ENST00000665070.1:c.565A>T	ENSP00000499482.1:p.Lys189Ter
ENST00000344887.9:c.532A>T	ENSP00000341838.5:p.Lys178Ter
ENST00000585806.5:n.531A>T
ENST00000588882.1:c.457A>T	ENSP00000466729.1:p.Lys153Ter
ENST00000589864.1:n.360A>T
NM_000363.4:c.532A>T , LRG_432t1:c.532A>T	NP_000354.4:p.Lys178Ter
NM_000363.5:c.532A>T MANE Select	NP_000354.4:p.Lys178Ter