Canonical Allele Identifier: CA2839180229

Gene: TNNI2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841594G>C , CM000673.2:g.1841594G>C	GRCh38
NC_000011.9:g.1862824G>C , CM000673.1:g.1862824G>C	GRCh37
NC_000011.8:g.1819400G>C	NCBI36
NG_011621.1:g.7592G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.*43G>C MANE Select	ENSP00000371336.1:n.*43G>C
ENST00000252898.11:c.592G>C	ENSP00000252898.7:n.592G>C
ENST00000381905.3:c.*43G>C	ENSP00000371330.3:n.*43G>C
ENST00000381906.5:c.*43G>C	ENSP00000371331.1:n.*43G>C
ENST00000381911.5:c.*43G>C	ENSP00000371336.1:n.*43G>C
ENST00000617947.4:c.*43G>C	ENSP00000481242.1:n.*43G>C
NM_001145829.1:c.*43G>C	NP_001139301.1:n.*43G>C
NM_001145841.1:c.*43G>C	NP_001139313.1:n.*43G>C
NM_003282.3:c.*43G>C	NP_003273.1:n.*43G>C
NM_003282.4:c.*43G>C MANE Select	NP_003273.1:n.*43G>C
NM_001145829.2:c.*43G>C	NP_001139301.1:n.*43G>C
NM_001145841.2:c.*43G>C	NP_001139313.1:n.*43G>C