Canonical Allele Identifier: CA513361409

Gene: TBX1

Linked Data

• gnomAD v4: 22-19765041-C-A
• COSMIC: COSM3414203 ; COSM3414204 ; COSM3414205
• MyVariant Identifiers: chr22:g.19752564C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19765041C>A , CM000684.2:g.19765041C>A	GRCh38
NC_000022.10:g.19752564C>A , CM000684.1:g.19752564C>A	GRCh37
NC_000022.9:g.18132564C>A	NCBI36
NG_009229.1:g.13339C>A , LRG_226:g.13339C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700274.1:c.321C>A	ENSP00000514909.1:p.Ala107=
ENST00000649276.2:c.795C>A MANE Select	ENSP00000497003.1:p.Ala265=
ENST00000329705.11:c.768C>A	ENSP00000331176.7:p.Ala256=
ENST00000332710.8:c.768C>A	ENSP00000331791.4:p.Ala256=
ENST00000359500.7:c.768C>A	ENSP00000352483.3:p.Ala256=
ENST00000621939.1:c.768C>A	ENSP00000477982.1:p.Ala256=
NM_005992.1:c.768C>A	NP_005983.1:p.Ala256=
NM_080646.1:c.768C>A	NP_542377.1:p.Ala256=
NM_080647.1:c.768C>A , LRG_226t1:c.768C>A	NP_542378.1:p.Ala256=
XM_006724312.1:c.768C>A	XP_006724375.1:p.Ala256=
XM_011530351.1:c.795C>A	XP_011528653.1:p.Ala265=
XM_006724312.2:c.768C>A	XP_006724375.1:p.Ala256=
XM_017028925.1:c.918C>A	XP_016884414.1:p.Ala306=
XM_017028926.1:c.768C>A	XP_016884415.1:p.Ala256=
XM_017028927.1:c.69C>A	XP_016884416.1:p.Ala23=
XM_017028928.1:c.918C>A	XP_016884417.1:p.Ala306=
NM_001379200.1:c.795C>A MANE Select	NP_001366129.1:p.Ala265=
NM_080646.2:c.768C>A	NP_542377.1:p.Ala256=