Canonical Allele Identifier: CA2439980763

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026780A= , CM000685.2:g.80026780A=	GRCh38
NC_000023.10:g.79282279A= , CM000685.1:g.79282279A=	GRCh37
NC_000023.9:g.79168935A=	NCBI36
NG_008998.1:g.17025A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.710A= MANE Select	ENSP00000362393.3:p.Gln237=
ENST00000373294.8:c.710A=	ENSP00000362390.5:p.Gln237=
ENST00000373296.7:c.710A=	ENSP00000362393.3:p.Gln237=
ENST00000626498.2:c.*322A=	ENSP00000487527.1:n.*322A=
ENST00000626877.1:n.589A=
NM_001109878.1:c.710A=	NP_001103348.1:p.Gln237=
NM_001109879.1:c.350A=	NP_001103349.1:p.Gln117=
NM_001303475.1:c.350A=	NP_001290404.1:p.Gln117=
NM_016954.2:c.710A=	NP_058650.1:p.Gln237=
XM_005262136.2:c.713A=	XP_005262193.1:p.Gln238=
XM_006724657.2:c.713A=	XP_006724720.1:p.Gln238=
XM_011530972.1:c.350A=	XP_011529274.1:p.Gln117=
NM_001109878.2:c.710A= MANE Select	NP_001103348.1:p.Gln237=
NM_001109879.2:c.350A=	NP_001103349.1:p.Gln117=