Canonical Allele Identifier: CA883720639

Gene: TNNI3

Linked Data

• dbSNP Id: rs1466812164
• gnomAD v3: 19-55152092-CCTGT-C
• gnomAD v4: 19-55152092-CCTGT-C
• MyVariant Identifiers: chr19:g.55663461_55663464del (hg19) ; chr19:g.55152093_55152096del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152095_55152098del , CM000681.2:g.55152095_55152098del	GRCh38
NC_000019.9:g.55663463_55663466del , CM000681.1:g.55663463_55663466del	GRCh37
NC_000019.8:g.60355275_60355278del	NCBI36
NG_007866.2:g.10637_10640del , LRG_432:g.10637_10640del
NG_011829.2:g.2143_2146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-179_550-176del MANE Select	ENSP00000341838.5:n.550-179_550-176del
ENST00000665070.1:c.583-179_583-176del	ENSP00000499482.1:n.583-179_583-176del
ENST00000344887.9:c.550-179_550-176del	ENSP00000341838.5:n.550-179_550-176del
ENST00000585806.5:n.549-179_549-176del
ENST00000588882.1:c.475-179_475-176del	ENSP00000466729.1:n.475-179_475-176del
ENST00000589864.1:n.378-179_378-176del
NM_000363.4:c.550-179_550-176del , LRG_432t1:c.550-179_550-176del	NP_000354.4:n.550-179_550-176del
NM_000363.5:c.550-179_550-176del MANE Select	NP_000354.4:n.550-179_550-176del