Canonical Allele Identifier: CA997261508

Gene: TNNI3

Linked Data

• dbSNP Id: rs2085717758
• gnomAD v3: 19-55154918-CCTGGACTCCTGGGTCTGAGGGAGGAGAAGGGGCTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGTTGGGGGCCTGGACTCCTGGGTTTGAGGGAGGAGAAGGGGCTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTGAGGGCCTCGATTCCAGGGTCTGAGGGAGGAGGGGCTGGGGA-C
• gnomAD v4: 19-55154918-CCTGGACTCCTGGGTCTGAGGGAGGAGAAGGGGCTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGTTGGGGGCCTGGACTCCTGGGTTTGAGGGAGGAGAAGGGGCTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTGAGGGCCTCGATTCCAGGGTCTGAGGGAGGAGGGGCTGGGGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154945_55155131del , CM000681.2:g.55154945_55155131del	GRCh38
NC_000019.9:g.55666313_55666499del , CM000681.1:g.55666313_55666499del	GRCh37
NC_000019.8:g.60358125_60358311del	NCBI36
NG_007866.2:g.7628_7814del , LRG_432:g.7628_7814del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.283-275_283-89del MANE Select	ENSP00000341838.5:n.283-275_283-89del
ENST00000665070.1:c.283-275_283-89del	ENSP00000499482.1:n.283-275_283-89del
ENST00000344887.9:c.283-275_283-89del	ENSP00000341838.5:n.283-275_283-89del
ENST00000585806.5:n.282-275_282-89del
ENST00000586669.5:n.291-275_291-89del
ENST00000587176.5:n.467-275_467-89del
ENST00000587871.1:c.902-275_902-89del
ENST00000588882.1:c.208-275_208-89del	ENSP00000466729.1:n.208-275_208-89del
ENST00000590463.1:n.455-275_455-89del
NM_000363.4:c.283-275_283-89del , LRG_432t1:c.283-275_283-89del	NP_000354.4:n.283-275_283-89del
NM_000363.5:c.283-275_283-89del MANE Select	NP_000354.4:n.283-275_283-89del