Canonical Allele Identifier: CA2396031422
Gene: TBX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19764983A= , CM000684.2:g.19764983A= GRCh38
NC_000022.10:g.19752506A= , CM000684.1:g.19752506A= GRCh37
NC_000022.9:g.18132506A= NCBI36
NG_009229.1:g.13281A= , LRG_226:g.13281A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.263A= ENSP00000514909.1:p.Tyr88=
ENST00000649276.2:c.737A= MANE Select ENSP00000497003.1:p.Tyr246=
ENST00000680333.1:c.710A= ENSP00000505472.1:p.Tyr237=
ENST00000329705.11:c.710A= ENSP00000331176.7:p.Tyr237=
ENST00000332710.8:c.710A= ENSP00000331791.4:p.Tyr237=
ENST00000359500.7:c.710A= ENSP00000352483.3:p.Tyr237=
ENST00000621939.1:c.710A= ENSP00000477982.1:p.Tyr237=
NM_005992.1:c.710A= NP_005983.1:p.Tyr237=
NM_080646.1:c.710A= NP_542377.1:p.Tyr237=
NM_080647.1:c.710A= , LRG_226t1:c.710A= NP_542378.1:p.Tyr237=
XM_006724312.1:c.710A= XP_006724375.1:p.Tyr237=
XM_011530351.1:c.737A= XP_011528653.1:p.Tyr246=
XM_006724312.2:c.710A= XP_006724375.1:p.Tyr237=
XM_017028925.1:c.860A= XP_016884414.1:p.Tyr287=
XM_017028926.1:c.710A= XP_016884415.1:p.Tyr237=
XM_017028927.1:c.11A= XP_016884416.1:p.Tyr4=
XM_017028928.1:c.860A= XP_016884417.1:p.Tyr287=
NM_001379200.1:c.737A= MANE Select NP_001366129.1:p.Tyr246=
NM_080646.2:c.710A= NP_542377.1:p.Tyr237=