Canonical Allele Identifier: CA2396032593
Gene: TBX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19766848A= , CM000684.2:g.19766848A= GRCh38
NC_000022.10:g.19754371A= , CM000684.1:g.19754371A= GRCh37
NC_000022.9:g.18134371A= NCBI36
NG_009229.1:g.15146A= , LRG_226:g.15146A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649276.2:c.1496A= MANE Select ENSP00000497003.1:p.Tyr499=
ENST00000329705.11:c.1009+846A= ENSP00000331176.7:n.1009+846A=
ENST00000332710.8:c.1469A= ENSP00000331791.4:p.Tyr490=
ENST00000359500.7:c.1009+846A= ENSP00000352483.3:n.1009+846A=
ENST00000621939.1:c.1009+846A= ENSP00000477982.1:n.1009+846A=
NM_005992.1:c.1009+846A= NP_005983.1:n.1009+846A=
NM_080646.1:c.1009+846A= NP_542377.1:n.1009+846A=
NM_080647.1:c.1469A= , LRG_226t1:c.1469A= NP_542378.1:p.Tyr490=
XM_006724312.1:c.1469A= XP_006724375.1:p.Tyr490=
XM_011530351.1:c.1496A= XP_011528653.1:p.Tyr499=
XM_006724312.2:c.1469A= XP_006724375.1:p.Tyr490=
XM_017028925.1:c.1619A= XP_016884414.1:p.Tyr540=
XM_017028926.1:c.1469A= XP_016884415.1:p.Tyr490=
XM_017028927.1:c.824A= XP_016884416.1:p.Tyr275=
XM_017028928.1:c.1159+846A= XP_016884417.1:n.1159+846A=
NM_001379200.1:c.1496A= MANE Select NP_001366129.1:p.Tyr499=
NM_080646.2:c.1009+846A= NP_542377.1:n.1009+846A=