Canonical Allele Identifier: CA410683325
Gene: TBX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19765008T>A , CM000684.2:g.19765008T>A GRCh38
NC_000022.10:g.19752531T>A , CM000684.1:g.19752531T>A GRCh37
NC_000022.9:g.18132531T>A NCBI36
NG_009229.1:g.13306T>A , LRG_226:g.13306T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.288T>A ENSP00000514909.1:p.Tyr96Ter
ENST00000649276.2:c.762T>A MANE Select ENSP00000497003.1:p.Tyr254Ter
ENST00000329705.11:c.735T>A ENSP00000331176.7:p.Tyr245Ter
ENST00000332710.8:c.735T>A ENSP00000331791.4:p.Tyr245Ter
ENST00000359500.7:c.735T>A ENSP00000352483.3:p.Tyr245Ter
ENST00000621939.1:c.735T>A ENSP00000477982.1:p.Tyr245Ter
NM_005992.1:c.735T>A NP_005983.1:p.Tyr245Ter
NM_080646.1:c.735T>A NP_542377.1:p.Tyr245Ter
NM_080647.1:c.735T>A , LRG_226t1:c.735T>A NP_542378.1:p.Tyr245Ter
XM_006724312.1:c.735T>A XP_006724375.1:p.Tyr245Ter
XM_011530351.1:c.762T>A XP_011528653.1:p.Tyr254Ter
XM_006724312.2:c.735T>A XP_006724375.1:p.Tyr245Ter
XM_017028925.1:c.885T>A XP_016884414.1:p.Tyr295Ter
XM_017028926.1:c.735T>A XP_016884415.1:p.Tyr245Ter
XM_017028927.1:c.36T>A XP_016884416.1:p.Tyr12Ter
XM_017028928.1:c.885T>A XP_016884417.1:p.Tyr295Ter
NM_001379200.1:c.762T>A MANE Select NP_001366129.1:p.Tyr254Ter
NM_080646.2:c.735T>A NP_542377.1:p.Tyr245Ter