Canonical Allele Identifier: CA2842288403

Gene: TNNI2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841578C>G , CM000673.2:g.1841578C>G	GRCh38
NC_000011.9:g.1862808C>G , CM000673.1:g.1862808C>G	GRCh37
NC_000011.8:g.1819384C>G	NCBI36
NG_011621.1:g.7576C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.*27C>G MANE Select	ENSP00000371336.1:n.*27C>G
ENST00000252898.11:c.576C>G	ENSP00000252898.7:n.576C>G
ENST00000381905.3:c.*27C>G	ENSP00000371330.3:n.*27C>G
ENST00000381906.5:c.*27C>G	ENSP00000371331.1:n.*27C>G
ENST00000381911.5:c.*27C>G	ENSP00000371336.1:n.*27C>G
ENST00000617947.4:c.*27C>G	ENSP00000481242.1:n.*27C>G
NM_001145829.1:c.*27C>G	NP_001139301.1:n.*27C>G
NM_001145841.1:c.*27C>G	NP_001139313.1:n.*27C>G
NM_003282.3:c.*27C>G	NP_003273.1:n.*27C>G
NM_003282.4:c.*27C>G MANE Select	NP_003273.1:n.*27C>G
NM_001145829.2:c.*27C>G	NP_001139301.1:n.*27C>G
NM_001145841.2:c.*27C>G	NP_001139313.1:n.*27C>G