Canonical Allele Identifier: CA410683298
Gene: TBX1 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19764996C>A , CM000684.2:g.19764996C>A GRCh38
NC_000022.10:g.19752519C>A , CM000684.1:g.19752519C>A GRCh37
NC_000022.9:g.18132519C>A NCBI36
NG_009229.1:g.13294C>A , LRG_226:g.13294C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.276C>A ENSP00000514909.1:p.Phe92Leu
ENST00000649276.2:c.750C>A MANE Select ENSP00000497003.1:p.Phe250Leu
ENST00000329705.11:c.723C>A ENSP00000331176.7:p.Phe241Leu
ENST00000332710.8:c.723C>A ENSP00000331791.4:p.Phe241Leu
ENST00000359500.7:c.723C>A ENSP00000352483.3:p.Phe241Leu
ENST00000621939.1:c.723C>A ENSP00000477982.1:p.Phe241Leu
NM_005992.1:c.723C>A NP_005983.1:p.Phe241Leu
NM_080646.1:c.723C>A NP_542377.1:p.Phe241Leu
NM_080647.1:c.723C>A , LRG_226t1:c.723C>A NP_542378.1:p.Phe241Leu
XM_006724312.1:c.723C>A XP_006724375.1:p.Phe241Leu
XM_011530351.1:c.750C>A XP_011528653.1:p.Phe250Leu
XM_006724312.2:c.723C>A XP_006724375.1:p.Phe241Leu
XM_017028925.1:c.873C>A XP_016884414.1:p.Phe291Leu
XM_017028926.1:c.723C>A XP_016884415.1:p.Phe241Leu
XM_017028927.1:c.24C>A XP_016884416.1:p.Phe8Leu
XM_017028928.1:c.873C>A XP_016884417.1:p.Phe291Leu
NM_001379200.1:c.750C>A MANE Select NP_001366129.1:p.Phe250Leu
NM_080646.2:c.723C>A NP_542377.1:p.Phe241Leu