Canonical Allele Identifier: CA407441256

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55666199C>T (hg19) ; chr19:g.55154831C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154831C>T , CM000681.2:g.55154831C>T	GRCh38
NC_000019.9:g.55666199C>T , CM000681.1:g.55666199C>T	GRCh37
NC_000019.8:g.60358011C>T	NCBI36
NG_007866.2:g.7902G>A , LRG_432:g.7902G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.283-1G>A MANE Select	ENSP00000341838.5:n.283-1G>A
ENST00000665070.1:c.283-1G>A	ENSP00000499482.1:n.283-1G>A
ENST00000344887.9:c.283-1G>A	ENSP00000341838.5:n.283-1G>A
ENST00000585806.5:n.282-1G>A
ENST00000586669.5:n.291-1G>A
ENST00000587176.5:n.467-1G>A
ENST00000587871.1:c.902-1G>A
ENST00000588882.1:c.208-1G>A	ENSP00000466729.1:n.208-1G>A
ENST00000590463.1:n.455-1G>A
NM_000363.4:c.283-1G>A , LRG_432t1:c.283-1G>A	NP_000354.4:n.283-1G>A
NM_000363.5:c.283-1G>A MANE Select	NP_000354.4:n.283-1G>A