Canonical Allele Identifier: CA310145076

Gene: TNNI3

Linked Data

• dbSNP Id: rs989065683
• gnomAD v3: 19-55152082-CCATGCACTTCCTGTCTCCCT-C
• gnomAD v4: 19-55152082-CCATGCACTTCCTGTCTCCCT-C
• MyVariant Identifiers: chr19:g.55663451_55663470del (hg19) ; chr19:g.55152083_55152102del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152098_55152117del , CM000681.2:g.55152098_55152117del	GRCh38
NC_000019.9:g.55663466_55663485del , CM000681.1:g.55663466_55663485del	GRCh37
NC_000019.8:g.60355278_60355297del	NCBI36
NG_007866.2:g.10631_10650del , LRG_432:g.10631_10650del
NG_011829.2:g.2137_2156del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-185_550-166del MANE Select	ENSP00000341838.5:n.550-185_550-166del
ENST00000665070.1:c.583-185_583-166del	ENSP00000499482.1:n.583-185_583-166del
ENST00000344887.9:c.550-185_550-166del	ENSP00000341838.5:n.550-185_550-166del
ENST00000585806.5:n.549-185_549-166del
ENST00000588882.1:c.475-185_475-166del	ENSP00000466729.1:n.475-185_475-166del
ENST00000589864.1:n.378-185_378-166del
NM_000363.4:c.550-185_550-166del , LRG_432t1:c.550-185_550-166del	NP_000354.4:n.550-185_550-166del
NM_000363.5:c.550-185_550-166del MANE Select	NP_000354.4:n.550-185_550-166del