Canonical Allele Identifier: CA883720670

Gene: TNNI3

Linked Data

• dbSNP Id: rs1334513488
• gnomAD v3: 19-55152168-ACTTT-A
• gnomAD v4: 19-55152168-ACTTT-A
• MyVariant Identifiers: chr19:g.55663537_55663540del (hg19) ; chr19:g.55152169_55152172del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152171_55152174del , CM000681.2:g.55152171_55152174del	GRCh38
NC_000019.9:g.55663539_55663542del , CM000681.1:g.55663539_55663542del	GRCh37
NC_000019.8:g.60355351_60355354del	NCBI36
NG_007866.2:g.10561_10564del , LRG_432:g.10561_10564del
NG_011829.2:g.2067_2070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-255_550-252del MANE Select	ENSP00000341838.5:n.550-255_550-252del
ENST00000665070.1:c.583-255_583-252del	ENSP00000499482.1:n.583-255_583-252del
ENST00000344887.9:c.550-255_550-252del	ENSP00000341838.5:n.550-255_550-252del
ENST00000585806.5:n.549-255_549-252del
ENST00000588882.1:c.475-255_475-252del	ENSP00000466729.1:n.475-255_475-252del
ENST00000589864.1:n.378-255_378-252del
NM_000363.4:c.550-255_550-252del , LRG_432t1:c.550-255_550-252del	NP_000354.4:n.550-255_550-252del
NM_000363.5:c.550-255_550-252del MANE Select	NP_000354.4:n.550-255_550-252del