Canonical Allele Identifier: CA310145028

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 1217767
• ClinVar RCV Id: RCV001590026
• dbSNP Id: rs542316818
• gnomAD v2: 19-55663390-C-CCTGT
• gnomAD v3: 19-55152022-C-CCTGT
• gnomAD v4: 19-55152022-C-CCTGT
• MyVariant Identifiers: chr19:g.55663390_55663391insCTGT (hg19) ; chr19:g.55152022_55152023insCTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152024_55152025insGTCT , CM000681.2:g.55152024_55152025insGTCT	GRCh38
NC_000019.9:g.55663392_55663393insGTCT , CM000681.1:g.55663392_55663393insGTCT	GRCh37
NC_000019.8:g.60355204_60355205insGTCT	NCBI36
NG_007866.2:g.10710_10711insACAG , LRG_432:g.10710_10711insACAG
NG_011829.2:g.2216_2217insACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-106_550-105insACAG MANE Select	ENSP00000341838.5:n.550-106_550-105insACAG
ENST00000665070.1:c.583-106_583-105insACAG	ENSP00000499482.1:n.583-106_583-105insACAG
ENST00000344887.9:c.550-106_550-105insACAG	ENSP00000341838.5:n.550-106_550-105insACAG
ENST00000585806.5:n.549-106_549-105insACAG
ENST00000588882.1:c.475-106_475-105insACAG	ENSP00000466729.1:n.475-106_475-105insACAG
ENST00000589864.1:n.378-106_378-105insACAG
NM_000363.4:c.550-106_550-105insACAG , LRG_432t1:c.550-106_550-105insACAG	NP_000354.4:n.550-106_550-105insACAG
NM_000363.5:c.550-106_550-105insACAG MANE Select	NP_000354.4:n.550-106_550-105insACAG