Canonical Allele Identifier: CA997261480

Gene: TNNI3

Linked Data

• dbSNP Id: rs2085717165
• gnomAD v4: 19-55154835-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154837del , CM000681.2:g.55154837del	GRCh38
NC_000019.9:g.55666205del , CM000681.1:g.55666205del	GRCh37
NC_000019.8:g.60358017del	NCBI36
NG_007866.2:g.7897del , LRG_432:g.7897del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.283-6del MANE Select	ENSP00000341838.5:n.283-6del
ENST00000665070.1:c.283-6del	ENSP00000499482.1:n.283-6del
ENST00000344887.9:c.283-6del	ENSP00000341838.5:n.283-6del
ENST00000585806.5:n.282-6del
ENST00000586669.5:n.291-6del
ENST00000587176.5:n.467-6del
ENST00000587871.1:c.902-6del
ENST00000588882.1:c.208-6del	ENSP00000466729.1:n.208-6del
ENST00000590463.1:n.455-6del
NM_000363.4:c.283-6del , LRG_432t1:c.283-6del	NP_000354.4:n.283-6del
NM_000363.5:c.283-6del MANE Select	NP_000354.4:n.283-6del