Canonical Allele Identifier: CA410683252
Gene: TBX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19764976C>T , CM000684.2:g.19764976C>T GRCh38
NC_000022.10:g.19752499C>T , CM000684.1:g.19752499C>T GRCh37
NC_000022.9:g.18132499C>T NCBI36
NG_009229.1:g.13274C>T , LRG_226:g.13274C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.256C>T ENSP00000514909.1:p.His86Tyr
ENST00000649276.2:c.730C>T MANE Select ENSP00000497003.1:p.His244Tyr
ENST00000680333.1:c.703C>T ENSP00000505472.1:p.His235Tyr
ENST00000329705.11:c.703C>T ENSP00000331176.7:p.His235Tyr
ENST00000332710.8:c.703C>T ENSP00000331791.4:p.His235Tyr
ENST00000359500.7:c.703C>T ENSP00000352483.3:p.His235Tyr
ENST00000621939.1:c.703C>T ENSP00000477982.1:p.His235Tyr
NM_005992.1:c.703C>T NP_005983.1:p.His235Tyr
NM_080646.1:c.703C>T NP_542377.1:p.His235Tyr
NM_080647.1:c.703C>T , LRG_226t1:c.703C>T NP_542378.1:p.His235Tyr
XM_006724312.1:c.703C>T XP_006724375.1:p.His235Tyr
XM_011530351.1:c.730C>T XP_011528653.1:p.His244Tyr
XM_006724312.2:c.703C>T XP_006724375.1:p.His235Tyr
XM_017028925.1:c.853C>T XP_016884414.1:p.His285Tyr
XM_017028926.1:c.703C>T XP_016884415.1:p.His235Tyr
XM_017028927.1:c.4C>T XP_016884416.1:p.His2Tyr
XM_017028928.1:c.853C>T XP_016884417.1:p.His285Tyr
NM_001379200.1:c.730C>T MANE Select NP_001366129.1:p.His244Tyr
NM_080646.2:c.703C>T NP_542377.1:p.His235Tyr