Canonical Allele Identifier: CA1947878890

Gene: TNNI2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841616A= , CM000673.2:g.1841616A=	GRCh38
NC_000011.9:g.1862846A= , CM000673.1:g.1862846A=	GRCh37
NC_000011.8:g.1819422A=	NCBI36
NG_011621.1:g.7614A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.*65A= MANE Select	ENSP00000371336.1:n.*65A=
ENST00000252898.11:c.614A=	ENSP00000252898.7:n.614A=
ENST00000381905.3:c.*65A=	ENSP00000371330.3:n.*65A=
ENST00000381906.5:c.*65A=	ENSP00000371331.1:n.*65A=
ENST00000381911.5:c.*65A=	ENSP00000371336.1:n.*65A=
ENST00000617947.4:c.*65A=	ENSP00000481242.1:n.*65A=
NM_001145829.1:c.*65A=	NP_001139301.1:n.*65A=
NM_001145841.1:c.*65A=	NP_001139313.1:n.*65A=
NM_003282.3:c.*65A=	NP_003273.1:n.*65A=
NM_003282.4:c.*65A= MANE Select	NP_003273.1:n.*65A=
NM_001145829.2:c.*65A=	NP_001139301.1:n.*65A=
NM_001145841.2:c.*65A=	NP_001139313.1:n.*65A=