Canonical Allele Identifier: CA410684815
Gene: TBX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19766633T>G , CM000684.2:g.19766633T>G GRCh38
NC_000022.10:g.19754156T>G , CM000684.1:g.19754156T>G GRCh37
NC_000022.9:g.18134156T>G NCBI36
NG_009229.1:g.14931T>G , LRG_226:g.14931T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649276.2:c.1281T>G MANE Select ENSP00000497003.1:p.Tyr427Ter
ENST00000329705.11:c.1009+631T>G ENSP00000331176.7:n.1009+631T>G
ENST00000332710.8:c.1254T>G ENSP00000331791.4:p.Tyr418Ter
ENST00000359500.7:c.1009+631T>G ENSP00000352483.3:n.1009+631T>G
ENST00000621939.1:c.1009+631T>G ENSP00000477982.1:n.1009+631T>G
NM_005992.1:c.1009+631T>G NP_005983.1:n.1009+631T>G
NM_080646.1:c.1009+631T>G NP_542377.1:n.1009+631T>G
NM_080647.1:c.1254T>G , LRG_226t1:c.1254T>G NP_542378.1:p.Tyr418Ter
XM_006724312.1:c.1254T>G XP_006724375.1:p.Tyr418Ter
XM_011530351.1:c.1281T>G XP_011528653.1:p.Tyr427Ter
XM_006724312.2:c.1254T>G XP_006724375.1:p.Tyr418Ter
XM_017028925.1:c.1404T>G XP_016884414.1:p.Tyr468Ter
XM_017028926.1:c.1254T>G XP_016884415.1:p.Tyr418Ter
XM_017028927.1:c.609T>G XP_016884416.1:p.Tyr203Ter
XM_017028928.1:c.1159+631T>G XP_016884417.1:n.1159+631T>G
NM_001379200.1:c.1281T>G MANE Select NP_001366129.1:p.Tyr427Ter
NM_080646.2:c.1009+631T>G NP_542377.1:n.1009+631T>G