Canonical Allele Identifier: CA2655307000

Gene: TBX1

Linked Data

• gnomAD v4: 22-19767019-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19767024del , CM000684.2:g.19767024del	GRCh38
NC_000022.10:g.19754547del , CM000684.1:g.19754547del	GRCh37
NC_000022.9:g.18134547del	NCBI36
NG_009229.1:g.15322del , LRG_226:g.15322del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649276.2:c.*157del MANE Select	ENSP00000497003.1:n.*157del
ENST00000329705.11:c.1009+1022del	ENSP00000331176.7:n.1009+1022del
ENST00000332710.8:c.*157del	ENSP00000331791.4:n.*157del
ENST00000359500.7:c.1009+1022del	ENSP00000352483.3:n.1009+1022del
ENST00000621939.1:c.1009+1022del	ENSP00000477982.1:n.1009+1022del
NM_005992.1:c.1009+1022del	NP_005983.1:n.1009+1022del
NM_080646.1:c.1009+1022del	NP_542377.1:n.1009+1022del
NM_080647.1:c.*157del , LRG_226t1:c.*157del	NP_542378.1:n.*157del
XM_006724312.1:c.*157del	XP_006724375.1:n.*157del
XM_011530351.1:c.*157del	XP_011528653.1:n.*157del
XM_006724312.2:c.*157del	XP_006724375.1:n.*157del
XM_017028925.1:c.*157del	XP_016884414.1:n.*157del
XM_017028926.1:c.*157del	XP_016884415.1:n.*157del
XM_017028927.1:c.*157del	XP_016884416.1:n.*157del
XM_017028928.1:c.1159+1022del	XP_016884417.1:n.1159+1022del
NM_001379200.1:c.*157del MANE Select	NP_001366129.1:n.*157del
NM_080646.2:c.1009+1022del	NP_542377.1:n.1009+1022del