Canonical Allele Identifier: CA310145114

Gene: TNNI3

Linked Data

• dbSNP Id: rs1020677653
• gnomAD v3: 19-55152098-TCCCTCATGCACTTCCTGTCC-T
• gnomAD v4: 19-55152098-TCCCTCATGCACTTCCTGTCC-T
• MyVariant Identifiers: chr19:g.55663467_55663486del (hg19) ; chr19:g.55152099_55152118del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152118_55152137del , CM000681.2:g.55152118_55152137del	GRCh38
NC_000019.9:g.55663486_55663505del , CM000681.1:g.55663486_55663505del	GRCh37
NC_000019.8:g.60355298_60355317del	NCBI36
NG_007866.2:g.10615_10634del , LRG_432:g.10615_10634del
NG_011829.2:g.2121_2140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-201_550-182del MANE Select	ENSP00000341838.5:n.550-201_550-182del
ENST00000665070.1:c.583-201_583-182del	ENSP00000499482.1:n.583-201_583-182del
ENST00000344887.9:c.550-201_550-182del	ENSP00000341838.5:n.550-201_550-182del
ENST00000585806.5:n.549-201_549-182del
ENST00000588882.1:c.475-201_475-182del	ENSP00000466729.1:n.475-201_475-182del
ENST00000589864.1:n.378-201_378-182del
NM_000363.4:c.550-201_550-182del , LRG_432t1:c.550-201_550-182del	NP_000354.4:n.550-201_550-182del
NM_000363.5:c.550-201_550-182del MANE Select	NP_000354.4:n.550-201_550-182del