Canonical Allele Identifier: CA2838961148

Gene: TNNI2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841558C>A , CM000673.2:g.1841558C>A	GRCh38
NC_000011.9:g.1862788C>A , CM000673.1:g.1862788C>A	GRCh37
NC_000011.8:g.1819364C>A	NCBI36
NG_011621.1:g.7556C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.*7C>A MANE Select	ENSP00000371336.1:n.*7C>A
ENST00000252898.11:c.556C>A	ENSP00000252898.7:n.556C>A
ENST00000381905.3:c.*7C>A	ENSP00000371330.3:n.*7C>A
ENST00000381906.5:c.*7C>A	ENSP00000371331.1:n.*7C>A
ENST00000381911.5:c.*7C>A	ENSP00000371336.1:n.*7C>A
ENST00000617947.4:c.*7C>A	ENSP00000481242.1:n.*7C>A
NM_001145829.1:c.*7C>A	NP_001139301.1:n.*7C>A
NM_001145841.1:c.*7C>A	NP_001139313.1:n.*7C>A
NM_003282.3:c.*7C>A	NP_003273.1:n.*7C>A
NM_003282.4:c.*7C>A MANE Select	NP_003273.1:n.*7C>A
NM_001145829.2:c.*7C>A	NP_001139301.1:n.*7C>A
NM_001145841.2:c.*7C>A	NP_001139313.1:n.*7C>A