Canonical Allele Identifier: CA410683292

Gene: TBX1

Linked Data

• MyVariant Identifiers: chr22:g.19752517T>A (hg19) ; chr22:g.19764994T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19764994T>A , CM000684.2:g.19764994T>A	GRCh38
NC_000022.10:g.19752517T>A , CM000684.1:g.19752517T>A	GRCh37
NC_000022.9:g.18132517T>A	NCBI36
NG_009229.1:g.13292T>A , LRG_226:g.13292T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700274.1:c.274T>A	ENSP00000514909.1:p.Phe92Ile
ENST00000649276.2:c.748T>A MANE Select	ENSP00000497003.1:p.Phe250Ile
ENST00000329705.11:c.721T>A	ENSP00000331176.7:p.Phe241Ile
ENST00000332710.8:c.721T>A	ENSP00000331791.4:p.Phe241Ile
ENST00000359500.7:c.721T>A	ENSP00000352483.3:p.Phe241Ile
ENST00000621939.1:c.721T>A	ENSP00000477982.1:p.Phe241Ile
NM_005992.1:c.721T>A	NP_005983.1:p.Phe241Ile
NM_080646.1:c.721T>A	NP_542377.1:p.Phe241Ile
NM_080647.1:c.721T>A , LRG_226t1:c.721T>A	NP_542378.1:p.Phe241Ile
XM_006724312.1:c.721T>A	XP_006724375.1:p.Phe241Ile
XM_011530351.1:c.748T>A	XP_011528653.1:p.Phe250Ile
XM_006724312.2:c.721T>A	XP_006724375.1:p.Phe241Ile
XM_017028925.1:c.871T>A	XP_016884414.1:p.Phe291Ile
XM_017028926.1:c.721T>A	XP_016884415.1:p.Phe241Ile
XM_017028927.1:c.22T>A	XP_016884416.1:p.Phe8Ile
XM_017028928.1:c.871T>A	XP_016884417.1:p.Phe291Ile
NM_001379200.1:c.748T>A MANE Select	NP_001366129.1:p.Phe250Ile
NM_080646.2:c.721T>A	NP_542377.1:p.Phe241Ile