Canonical Allele Identifier: CA1947877269

Gene: TNNI2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1840531G= , CM000673.2:g.1840531G=	GRCh38
NC_000011.9:g.1861761G= , CM000673.1:g.1861761G=	GRCh37
NC_000011.8:g.1818337G=	NCBI36
NG_011621.1:g.6529G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.61G= MANE Select	ENSP00000371336.1:p.Val21=
ENST00000252898.11:c.61G=	ENSP00000252898.7:p.Val21=
ENST00000381905.3:c.61G=	ENSP00000371330.3:p.Val21=
ENST00000381906.5:c.61G=	ENSP00000371331.1:p.Val21=
ENST00000381911.5:c.61G=	ENSP00000371336.1:p.Val21=
ENST00000468473.1:n.231G=
ENST00000617947.4:c.61G=	ENSP00000481242.1:p.Val21=
NM_001145829.1:c.61G=	NP_001139301.1:p.Val21=
NM_001145841.1:c.61G=	NP_001139313.1:p.Val21=
NM_003282.3:c.61G=	NP_003273.1:p.Val21=
NM_003282.4:c.61G= MANE Select	NP_003273.1:p.Val21=
NM_001145829.2:c.61G=	NP_001139301.1:p.Val21=
NM_001145841.2:c.61G=	NP_001139313.1:p.Val21=