Canonical Allele Identifier: CA407440936

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55666120T>A (hg19) ; chr19:g.55154752T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154752T>A , CM000681.2:g.55154752T>A	GRCh38
NC_000019.9:g.55666120T>A , CM000681.1:g.55666120T>A	GRCh37
NC_000019.8:g.60357932T>A	NCBI36
NG_007866.2:g.7981A>T , LRG_432:g.7981A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.361A>T MANE Select	ENSP00000341838.5:p.Asn121Tyr
ENST00000665070.1:c.361A>T	ENSP00000499482.1:p.Asn121Tyr
ENST00000344887.9:c.361A>T	ENSP00000341838.5:p.Asn121Tyr
ENST00000585806.5:n.360A>T
ENST00000586669.5:n.369A>T
ENST00000587176.5:n.545A>T
ENST00000588882.1:c.286A>T	ENSP00000466729.1:p.Asn96Tyr
ENST00000590463.1:n.533A>T
NM_000363.4:c.361A>T , LRG_432t1:c.361A>T	NP_000354.4:p.Asn121Tyr
NM_000363.5:c.361A>T MANE Select	NP_000354.4:p.Asn121Tyr