Canonical Allele Identifier: CA9667715

Gene: TNNI3

Linked Data

• dbSNP Id: rs777744715
• ExAC: 19:55663158 TTCCTCAGGGCCC / T
• gnomAD v2: 19-55663158-TTCCTCAGGGCCC-T
• gnomAD v4: 19-55151790-TTCCTCAGGGCCC-T
• MyVariant Identifiers: chr19:g.55663159_55663170del (hg19) ; chr19:g.55151791_55151802del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151801_55151812del , CM000681.2:g.55151801_55151812del	GRCh38
NC_000019.9:g.55663169_55663180del , CM000681.1:g.55663169_55663180del	GRCh37
NC_000019.8:g.60354981_60354992del	NCBI36
NG_007866.2:g.10931_10942del , LRG_432:g.10931_10942del
NG_011829.2:g.2437_2448del

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.*32_*43del MANE Select	ENSP00000341838.5:n.*32_*43del
ENST00000665070.1:c.*32_*43del	ENSP00000499482.1:n.*32_*43del
ENST00000344887.9:c.*32_*43del	ENSP00000341838.5:n.*32_*43del
ENST00000585806.5:n.664_675del
ENST00000588882.1:c.*32_*43del	ENSP00000466729.1:n.*32_*43del
ENST00000589864.1:n.493_504del
NM_000363.4:c.*32_*43del , LRG_432t1:c.*32_*43del	NP_000354.4:n.*32_*43del
NM_000363.5:c.*32_*43del MANE Select	NP_000354.4:n.*32_*43del