Canonical Allele Identifier: CA883723390

Gene: TNNI3

Linked Data

• dbSNP Id: rs1249390440
• gnomAD v3: 19-55154900-GGGAGAAGGGGCTCGGGGCCTGGACTCCTGGGTCTGAGGGA-G
• gnomAD v4: 19-55154900-GGGAGAAGGGGCTCGGGGCCTGGACTCCTGGGTCTGAGGGA-G
• MyVariant Identifiers: chr19:g.55666269_55666308del (hg19) ; chr19:g.55154901_55154940del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154913_55154952del , CM000681.2:g.55154913_55154952del	GRCh38
NC_000019.9:g.55666281_55666320del , CM000681.1:g.55666281_55666320del	GRCh37
NC_000019.8:g.60358093_60358132del	NCBI36
NG_007866.2:g.7793_7832del , LRG_432:g.7793_7832del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.283-110_283-71del MANE Select	ENSP00000341838.5:n.283-110_283-71del
ENST00000665070.1:c.283-110_283-71del	ENSP00000499482.1:n.283-110_283-71del
ENST00000344887.9:c.283-110_283-71del	ENSP00000341838.5:n.283-110_283-71del
ENST00000585806.5:n.282-110_282-71del
ENST00000586669.5:n.291-110_291-71del
ENST00000587176.5:n.467-110_467-71del
ENST00000587871.1:c.902-110_902-71del
ENST00000588882.1:c.208-110_208-71del	ENSP00000466729.1:n.208-110_208-71del
ENST00000590463.1:n.455-110_455-71del
NM_000363.4:c.283-110_283-71del , LRG_432t1:c.283-110_283-71del	NP_000354.4:n.283-110_283-71del
NM_000363.5:c.283-110_283-71del MANE Select	NP_000354.4:n.283-110_283-71del