Canonical Allele Identifier: CA633870561

Gene: TNNI3

Linked Data

• dbSNP Id: rs1272706972
• gnomAD v2: 19-55663626-CT-C
• gnomAD v3: 19-55152258-CT-C
• gnomAD v4: 19-55152258-CT-C
• MyVariant Identifiers: chr19:g.55663627del (hg19) ; chr19:g.55152259del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152261del , CM000681.2:g.55152261del	GRCh38
NC_000019.9:g.55663629del , CM000681.1:g.55663629del	GRCh37
NC_000019.8:g.60355441del	NCBI36
NG_007866.2:g.10474del , LRG_432:g.10474del
NG_011829.2:g.1980del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-342del MANE Select	ENSP00000341838.5:n.550-342del
ENST00000665070.1:c.583-342del	ENSP00000499482.1:n.583-342del
ENST00000344887.9:c.550-342del	ENSP00000341838.5:n.550-342del
ENST00000585806.5:n.549-342del
ENST00000588882.1:c.475-342del	ENSP00000466729.1:n.475-342del
ENST00000589864.1:n.378-342del
NM_000363.4:c.550-342del , LRG_432t1:c.550-342del	NP_000354.4:n.550-342del
NM_000363.5:c.550-342del MANE Select	NP_000354.4:n.550-342del