Canonical Allele Identifier: CA1947877323

Gene: TNNI2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1840577_1840578delinsGC , CM000673.2:g.1840577_1840578delinsGC	GRCh38
NC_000011.9:g.1861807_1861808delinsGC , CM000673.1:g.1861807_1861808delinsGC	GRCh37
NC_000011.8:g.1818383_1818384delinsGC	NCBI36
NG_011621.1:g.6575_6576delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.107_108delinsGC MANE Select	ENSP00000371336.1:p.Arg36=
ENST00000252898.11:c.107_108delinsGC	ENSP00000252898.7:p.Arg36=
ENST00000381905.3:c.107_108delinsGC	ENSP00000371330.3:p.Arg36=
ENST00000381906.5:c.107_108delinsGC	ENSP00000371331.1:p.Arg36=
ENST00000381911.5:c.107_108delinsGC	ENSP00000371336.1:p.Arg36=
ENST00000468473.1:n.277_278delinsGC
ENST00000617947.4:c.107_108delinsGC	ENSP00000481242.1:p.Arg36=
NM_001145829.1:c.107_108delinsGC	NP_001139301.1:p.Arg36=
NM_001145841.1:c.107_108delinsGC	NP_001139313.1:p.Arg36=
NM_003282.3:c.107_108delinsGC	NP_003273.1:p.Arg36=
NM_003282.4:c.107_108delinsGC MANE Select	NP_003273.1:p.Arg36=
NM_001145829.2:c.107_108delinsGC	NP_001139301.1:p.Arg36=
NM_001145841.2:c.107_108delinsGC	NP_001139313.1:p.Arg36=