Canonical Allele Identifier: CA413740783

Gene: TBX22

Linked Data

• MyVariant Identifiers: chrX:g.79282281A>T (hg19) ; chrX:g.80026782A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026782A>T , CM000685.2:g.80026782A>T	GRCh38
NC_000023.10:g.79282281A>T , CM000685.1:g.79282281A>T	GRCh37
NC_000023.9:g.79168937A>T	NCBI36
NG_008998.1:g.17027A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.712A>T MANE Select	ENSP00000362393.3:p.Ile238Phe
ENST00000373294.8:c.712A>T	ENSP00000362390.5:p.Ile238Phe
ENST00000373296.7:c.712A>T	ENSP00000362393.3:p.Ile238Phe
ENST00000626498.2:c.*324A>T	ENSP00000487527.1:n.*324A>T
ENST00000626877.1:n.591A>T
NM_001109878.1:c.712A>T	NP_001103348.1:p.Ile238Phe
NM_001109879.1:c.352A>T	NP_001103349.1:p.Ile118Phe
NM_001303475.1:c.352A>T	NP_001290404.1:p.Ile118Phe
NM_016954.2:c.712A>T	NP_058650.1:p.Ile238Phe
XM_005262136.2:c.715A>T	XP_005262193.1:p.Ile239Phe
XM_006724657.2:c.715A>T	XP_006724720.1:p.Ile239Phe
XM_011530972.1:c.352A>T	XP_011529274.1:p.Ile118Phe
NM_001109878.2:c.712A>T MANE Select	NP_001103348.1:p.Ile238Phe
NM_001109879.2:c.352A>T	NP_001103349.1:p.Ile118Phe