Canonical Allele Identifier: CA883723121

Gene: TNNI3

Linked Data

• dbSNP Id: rs1181373184
• MyVariant Identifiers: chr19:g.55666160_55666170del (hg19) ; chr19:g.55154792_55154802del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154795_55154805del , CM000681.2:g.55154795_55154805del	GRCh38
NC_000019.9:g.55666163_55666173del , CM000681.1:g.55666163_55666173del	GRCh37
NC_000019.8:g.60357975_60357985del	NCBI36
NG_007866.2:g.7931_7941del , LRG_432:g.7931_7941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.311_321del MANE Select	ENSP00000341838.5:p.Val104GlyfsTer2
ENST00000665070.1:c.311_321del	ENSP00000499482.1:p.Val104GlyfsTer2
ENST00000344887.9:c.311_321del	ENSP00000341838.5:p.Val104GlyfsTer2
ENST00000585806.5:n.310_320del
ENST00000586669.5:n.319_329del
ENST00000587176.5:n.495_505del
ENST00000587871.1:c.930_940del
ENST00000588882.1:c.236_246del	ENSP00000466729.1:p.Val79GlyfsTer2
ENST00000590463.1:n.483_493del
NM_000363.4:c.311_321del , LRG_432t1:c.311_321del	NP_000354.4:p.Val104GlyfsTer2
NM_000363.5:c.311_321del MANE Select	NP_000354.4:p.Val104GlyfsTer2