Canonical Allele Identifier: CA633870549

Gene: TNNI3

Linked Data

• dbSNP Id: rs1350448131
• gnomAD v2: 19-55663545-CT-C
• gnomAD v3: 19-55152177-CT-C
• gnomAD v4: 19-55152177-CT-C
• MyVariant Identifiers: chr19:g.55663546del (hg19) ; chr19:g.55152178del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152180del , CM000681.2:g.55152180del	GRCh38
NC_000019.9:g.55663548del , CM000681.1:g.55663548del	GRCh37
NC_000019.8:g.60355360del	NCBI36
NG_007866.2:g.10555del , LRG_432:g.10555del
NG_011829.2:g.2061del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-261del MANE Select	ENSP00000341838.5:n.550-261del
ENST00000665070.1:c.583-261del	ENSP00000499482.1:n.583-261del
ENST00000344887.9:c.550-261del	ENSP00000341838.5:n.550-261del
ENST00000585806.5:n.549-261del
ENST00000588882.1:c.475-261del	ENSP00000466729.1:n.475-261del
ENST00000589864.1:n.378-261del
NM_000363.4:c.550-261del , LRG_432t1:c.550-261del	NP_000354.4:n.550-261del
NM_000363.5:c.550-261del MANE Select	NP_000354.4:n.550-261del