Canonical Allele Identifier: CA2655306507

Gene: TBX1

Linked Data

• gnomAD v4: 22-19766624-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19766625del , CM000684.2:g.19766625del	GRCh38
NC_000022.10:g.19754148del , CM000684.1:g.19754148del	GRCh37
NC_000022.9:g.18134148del	NCBI36
NG_009229.1:g.14923del , LRG_226:g.14923del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649276.2:c.1273del MANE Select	ENSP00000497003.1:p.Tyr425ThrfsTer?
ENST00000329705.11:c.1009+623del	ENSP00000331176.7:n.1009+623del
ENST00000332710.8:c.1246del	ENSP00000331791.4:p.Tyr416ThrfsTer?
ENST00000359500.7:c.1009+623del	ENSP00000352483.3:n.1009+623del
ENST00000621939.1:c.1009+623del	ENSP00000477982.1:n.1009+623del
NM_005992.1:c.1009+623del	NP_005983.1:n.1009+623del
NM_080646.1:c.1009+623del	NP_542377.1:n.1009+623del
NM_080647.1:c.1246del , LRG_226t1:c.1246del	NP_542378.1:p.Tyr416ThrfsTer?
XM_006724312.1:c.1246del	XP_006724375.1:p.Tyr416ThrfsTer?
XM_011530351.1:c.1273del	XP_011528653.1:p.Tyr425ThrfsTer?
XM_006724312.2:c.1246del	XP_006724375.1:p.Tyr416ThrfsTer?
XM_017028925.1:c.1396del	XP_016884414.1:p.Tyr466ThrfsTer?
XM_017028926.1:c.1246del	XP_016884415.1:p.Tyr416ThrfsTer?
XM_017028927.1:c.601del	XP_016884416.1:p.Tyr201ThrfsTer?
XM_017028928.1:c.1159+623del	XP_016884417.1:n.1159+623del
NM_001379200.1:c.1273del MANE Select	NP_001366129.1:p.Tyr425ThrfsTer?
NM_080646.2:c.1009+623del	NP_542377.1:n.1009+623del