Canonical Allele Identifier: CA410682968
Gene: TBX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19764259G>A , CM000684.2:g.19764259G>A GRCh38
NC_000022.10:g.19751782G>A , CM000684.1:g.19751782G>A GRCh37
NC_000022.9:g.18131782G>A NCBI36
NG_009229.1:g.12557G>A , LRG_226:g.12557G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.170G>A ENSP00000514909.1:p.Trp57Ter
ENST00000649276.2:c.644G>A MANE Select ENSP00000497003.1:p.Trp215Ter
ENST00000680333.1:c.617G>A ENSP00000505472.1:p.Trp206Ter
ENST00000329705.11:c.617G>A ENSP00000331176.7:p.Trp206Ter
ENST00000332710.8:c.617G>A ENSP00000331791.4:p.Trp206Ter
ENST00000359500.7:c.617G>A ENSP00000352483.3:p.Trp206Ter
ENST00000621939.1:c.617G>A ENSP00000477982.1:p.Trp206Ter
NM_005992.1:c.617G>A NP_005983.1:p.Trp206Ter
NM_080646.1:c.617G>A NP_542377.1:p.Trp206Ter
NM_080647.1:c.617G>A , LRG_226t1:c.617G>A NP_542378.1:p.Trp206Ter
XM_006724312.1:c.617G>A XP_006724375.1:p.Trp206Ter
XM_011530351.1:c.644G>A XP_011528653.1:p.Trp215Ter
XM_006724312.2:c.617G>A XP_006724375.1:p.Trp206Ter
XM_017028925.1:c.767G>A XP_016884414.1:p.Trp256Ter
XM_017028926.1:c.617G>A XP_016884415.1:p.Trp206Ter
XM_017028928.1:c.767G>A XP_016884417.1:p.Trp256Ter
NM_001379200.1:c.644G>A MANE Select NP_001366129.1:p.Trp215Ter
NM_080646.2:c.617G>A NP_542377.1:p.Trp206Ter