Canonical Allele Identifier: CA1947878773

Gene: TNNI2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841523_1841526delinsGGAA , CM000673.2:g.1841523_1841526delinsGGAA	GRCh38
NC_000011.9:g.1862753_1862756delinsGGAA , CM000673.1:g.1862753_1862756delinsGGAA	GRCh37
NC_000011.8:g.1819329_1819332delinsGGAA	NCBI36
NG_011621.1:g.7521_7524delinsGGAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000381911.6:c.521_524delinsGGAA MANE Select	ENSP00000371336.1:p.Arg174=
ENST00000252898.11:c.521_524delinsGGAA	ENSP00000252898.7:p.Arg174=
ENST00000381905.3:c.521_524delinsGGAA	ENSP00000371330.3:p.Arg174=
ENST00000381906.5:c.521_524delinsGGAA	ENSP00000371331.1:p.Arg174=
ENST00000381911.5:c.521_524delinsGGAA	ENSP00000371336.1:p.Arg174=
ENST00000617947.4:c.521_524delinsGGAA	ENSP00000481242.1:p.Arg174=
NM_001145829.1:c.521_524delinsGGAA	NP_001139301.1:p.Arg174=
NM_001145841.1:c.521_524delinsGGAA	NP_001139313.1:p.Arg174=
NM_003282.3:c.521_524delinsGGAA	NP_003273.1:p.Arg174=
NM_003282.4:c.521_524delinsGGAA MANE Select	NP_003273.1:p.Arg174=
NM_001145829.2:c.521_524delinsGGAA	NP_001139301.1:p.Arg174=
NM_001145841.2:c.521_524delinsGGAA	NP_001139313.1:p.Arg174=