Canonical Allele Identifier: CA2840052003

Gene: TNNI2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841590C>A , CM000673.2:g.1841590C>A	GRCh38
NC_000011.9:g.1862820C>A , CM000673.1:g.1862820C>A	GRCh37
NC_000011.8:g.1819396C>A	NCBI36
NG_011621.1:g.7588C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.*39C>A MANE Select	ENSP00000371336.1:n.*39C>A
ENST00000252898.11:c.588C>A	ENSP00000252898.7:n.588C>A
ENST00000381905.3:c.*39C>A	ENSP00000371330.3:n.*39C>A
ENST00000381906.5:c.*39C>A	ENSP00000371331.1:n.*39C>A
ENST00000381911.5:c.*39C>A	ENSP00000371336.1:n.*39C>A
ENST00000617947.4:c.*39C>A	ENSP00000481242.1:n.*39C>A
NM_001145829.1:c.*39C>A	NP_001139301.1:n.*39C>A
NM_001145841.1:c.*39C>A	NP_001139313.1:n.*39C>A
NM_003282.3:c.*39C>A	NP_003273.1:n.*39C>A
NM_003282.4:c.*39C>A MANE Select	NP_003273.1:n.*39C>A
NM_001145829.2:c.*39C>A	NP_001139301.1:n.*39C>A
NM_001145841.2:c.*39C>A	NP_001139313.1:n.*39C>A