Canonical Allele Identifier: CA674310532

Gene: TNNI2

Linked Data

• dbSNP Id: rs1468713591
• gnomAD v4: 11-1841305-CG-C
• MyVariant Identifiers: chr11:g.1862536del (hg19) ; chr11:g.1841306del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841310del , CM000673.2:g.1841310del	GRCh38
NC_000011.9:g.1862540del , CM000673.1:g.1862540del	GRCh37
NC_000011.8:g.1819116del	NCBI36
NG_011621.1:g.7308del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.453+103del MANE Select	ENSP00000371336.1:n.453+103del
ENST00000252898.11:c.453+103del	ENSP00000252898.7:n.453+103del
ENST00000381905.3:c.453+103del	ENSP00000371330.3:n.453+103del
ENST00000381906.5:c.453+103del	ENSP00000371331.1:n.453+103del
ENST00000381911.5:c.453+103del	ENSP00000371336.1:n.453+103del
ENST00000617947.4:c.453+103del	ENSP00000481242.1:n.453+103del
NM_001145829.1:c.453+103del	NP_001139301.1:n.453+103del
NM_001145841.1:c.453+103del	NP_001139313.1:n.453+103del
NM_003282.3:c.453+103del	NP_003273.1:n.453+103del
NM_003282.4:c.453+103del MANE Select	NP_003273.1:n.453+103del
NM_001145829.2:c.453+103del	NP_001139301.1:n.453+103del
NM_001145841.2:c.453+103del	NP_001139313.1:n.453+103del