Canonical Allele Identifier: CA410683257
Gene: TBX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19764978C>G , CM000684.2:g.19764978C>G GRCh38
NC_000022.10:g.19752501C>G , CM000684.1:g.19752501C>G GRCh37
NC_000022.9:g.18132501C>G NCBI36
NG_009229.1:g.13276C>G , LRG_226:g.13276C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000700274.1:c.258C>G ENSP00000514909.1:p.His86Gln
ENST00000649276.2:c.732C>G MANE Select ENSP00000497003.1:p.His244Gln
ENST00000680333.1:c.705C>G ENSP00000505472.1:p.His235Gln
ENST00000329705.11:c.705C>G ENSP00000331176.7:p.His235Gln
ENST00000332710.8:c.705C>G ENSP00000331791.4:p.His235Gln
ENST00000359500.7:c.705C>G ENSP00000352483.3:p.His235Gln
ENST00000621939.1:c.705C>G ENSP00000477982.1:p.His235Gln
NM_005992.1:c.705C>G NP_005983.1:p.His235Gln
NM_080646.1:c.705C>G NP_542377.1:p.His235Gln
NM_080647.1:c.705C>G , LRG_226t1:c.705C>G NP_542378.1:p.His235Gln
XM_006724312.1:c.705C>G XP_006724375.1:p.His235Gln
XM_011530351.1:c.732C>G XP_011528653.1:p.His244Gln
XM_006724312.2:c.705C>G XP_006724375.1:p.His235Gln
XM_017028925.1:c.855C>G XP_016884414.1:p.His285Gln
XM_017028926.1:c.705C>G XP_016884415.1:p.His235Gln
XM_017028927.1:c.6C>G XP_016884416.1:p.His2Gln
XM_017028928.1:c.855C>G XP_016884417.1:p.His285Gln
NM_001379200.1:c.732C>G MANE Select NP_001366129.1:p.His244Gln
NM_080646.2:c.705C>G NP_542377.1:p.His235Gln