Canonical Allele Identifier: CA1947877324
Gene: TNNI2 HGNC NCBI

Linked Data

dbSNP Id: rs1847144162

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1840579del , CM000673.2:g.1840579del GRCh38
NC_000011.9:g.1861809del , CM000673.1:g.1861809del GRCh37
NC_000011.8:g.1818385del NCBI36
NG_011621.1:g.6577del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381911.6:c.109del MANE Select ENSP00000371336.1:p.Arg37ValfsTer?
ENST00000252898.11:c.109del ENSP00000252898.7:p.Arg37ValfsTer?
ENST00000381905.3:c.109del ENSP00000371330.3:p.Arg37ValfsTer?
ENST00000381906.5:c.109del ENSP00000371331.1:p.Arg37ValfsTer?
ENST00000381911.5:c.109del ENSP00000371336.1:p.Arg37ValfsTer?
ENST00000468473.1:n.279del
ENST00000617947.4:c.109del ENSP00000481242.1:p.Arg37ValfsTer?
NM_001145829.1:c.109del NP_001139301.1:p.Arg37ValfsTer?
NM_001145841.1:c.109del NP_001139313.1:p.Arg37ValfsTer?
NM_003282.3:c.109del NP_003273.1:p.Arg37ValfsTer?
NM_003282.4:c.109del MANE Select NP_003273.1:p.Arg37ValfsTer?
NM_001145829.2:c.109del NP_001139301.1:p.Arg37ValfsTer?
NM_001145841.2:c.109del NP_001139313.1:p.Arg37ValfsTer?