Canonical Allele Identifier: CA10102565
Gene: TBX1 HGNC NCBI

Linked Data

dbSNP Id: rs767591426

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19765071G>A , CM000684.2:g.19765071G>A GRCh38
NC_000022.10:g.19752594G>A , CM000684.1:g.19752594G>A GRCh37
NC_000022.9:g.18132594G>A NCBI36
NG_009229.1:g.13369G>A , LRG_226:g.13369G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.351G>A ENSP00000514909.1:p.Glu117=
ENST00000649276.2:c.825G>A MANE Select ENSP00000497003.1:p.Glu275=
ENST00000329705.11:c.798G>A ENSP00000331176.7:p.Glu266=
ENST00000332710.8:c.798G>A ENSP00000331791.4:p.Glu266=
ENST00000359500.7:c.798G>A ENSP00000352483.3:p.Glu266=
ENST00000621939.1:c.798G>A ENSP00000477982.1:p.Glu266=
NM_005992.1:c.798G>A NP_005983.1:p.Glu266=
NM_080646.1:c.798G>A NP_542377.1:p.Glu266=
NM_080647.1:c.798G>A , LRG_226t1:c.798G>A NP_542378.1:p.Glu266=
XM_006724312.1:c.798G>A XP_006724375.1:p.Glu266=
XM_011530351.1:c.825G>A XP_011528653.1:p.Glu275=
XM_006724312.2:c.798G>A XP_006724375.1:p.Glu266=
XM_017028925.1:c.948G>A XP_016884414.1:p.Glu316=
XM_017028926.1:c.798G>A XP_016884415.1:p.Glu266=
XM_017028927.1:c.99G>A XP_016884416.1:p.Glu33=
XM_017028928.1:c.948G>A XP_016884417.1:p.Glu316=
NM_001379200.1:c.825G>A MANE Select NP_001366129.1:p.Glu275=
NM_080646.2:c.798G>A NP_542377.1:p.Glu266=