Canonical Allele Identifier: CA633871300

Gene: TNNI3

Linked Data

• dbSNP Id: rs2085717690
• gnomAD v2: 19-55666281-CGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGAAGGGGCTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGTTGGGGGCCTGGACTCCTGGGTTTGAGGGAGGAGAAGGGGCTG-C
• gnomAD v3: 19-55154913-CGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGAAGGGGCTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGTTGGGGGCCTGGACTCCTGGGTTTGAGGGAGGAGAAGGGGCTG-C
• gnomAD v4: 19-55154913-CGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGAAGGGGCTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGTTGGGGGCCTGGACTCCTGGGTTTGAGGGAGGAGAAGGGGCTG-C
• MyVariant Identifiers: chr19:g.55666282_55666395del (hg19) ; chr19:g.55154914_55155027del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154945_55155058del , CM000681.2:g.55154945_55155058del	GRCh38
NC_000019.9:g.55666313_55666426del , CM000681.1:g.55666313_55666426del	GRCh37
NC_000019.8:g.60358125_60358238del	NCBI36
NG_007866.2:g.7706_7819del , LRG_432:g.7706_7819del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.283-197_283-84del MANE Select	ENSP00000341838.5:n.283-197_283-84del
ENST00000665070.1:c.283-197_283-84del	ENSP00000499482.1:n.283-197_283-84del
ENST00000344887.9:c.283-197_283-84del	ENSP00000341838.5:n.283-197_283-84del
ENST00000585806.5:n.282-197_282-84del
ENST00000586669.5:n.291-197_291-84del
ENST00000587176.5:n.467-197_467-84del
ENST00000587871.1:c.902-197_902-84del
ENST00000588882.1:c.208-197_208-84del	ENSP00000466729.1:n.208-197_208-84del
ENST00000590463.1:n.455-197_455-84del
NM_000363.4:c.283-197_283-84del , LRG_432t1:c.283-197_283-84del	NP_000354.4:n.283-197_283-84del
NM_000363.5:c.283-197_283-84del MANE Select	NP_000354.4:n.283-197_283-84del