Canonical Allele Identifier: CA2790176643

Gene: TNNI2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1840570_1840572del , CM000673.2:g.1840570_1840572del	GRCh38
NC_000011.9:g.1861800_1861802del , CM000673.1:g.1861800_1861802del	GRCh37
NC_000011.8:g.1818376_1818378del	NCBI36
NG_011621.1:g.6568_6570del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.100_102del MANE Select	ENSP00000371336.1:p.Glu34del
ENST00000252898.11:c.100_102del	ENSP00000252898.7:p.Glu34del
ENST00000381905.3:c.100_102del	ENSP00000371330.3:p.Glu34del
ENST00000381906.5:c.100_102del	ENSP00000371331.1:p.Glu34del
ENST00000381911.5:c.100_102del	ENSP00000371336.1:p.Glu34del
ENST00000468473.1:n.270_272del
ENST00000617947.4:c.100_102del	ENSP00000481242.1:p.Glu34del
NM_001145829.1:c.100_102del	NP_001139301.1:p.Glu34del
NM_001145841.1:c.100_102del	NP_001139313.1:p.Glu34del
NM_003282.3:c.100_102del	NP_003273.1:p.Glu34del
NM_003282.4:c.100_102del MANE Select	NP_003273.1:p.Glu34del
NM_001145829.2:c.100_102del	NP_001139301.1:p.Glu34del
NM_001145841.2:c.100_102del	NP_001139313.1:p.Glu34del