Canonical Allele Identifier: CA2396031461
Gene: TBX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19765083C= , CM000684.2:g.19765083C= GRCh38
NC_000022.10:g.19752606C= , CM000684.1:g.19752606C= GRCh37
NC_000022.9:g.18132606C= NCBI36
NG_009229.1:g.13381C= , LRG_226:g.13381C=

Transcript Alleles

HGVS Amino-acid change
ENST00000700274.1:c.363C= ENSP00000514909.1:p.Phe121=
ENST00000649276.2:c.837C= MANE Select ENSP00000497003.1:p.Phe279=
ENST00000329705.11:c.810C= ENSP00000331176.7:p.Phe270=
ENST00000332710.8:c.810C= ENSP00000331791.4:p.Phe270=
ENST00000359500.7:c.810C= ENSP00000352483.3:p.Phe270=
ENST00000484336.1:n.5C=
ENST00000621939.1:c.810C= ENSP00000477982.1:p.Phe270=
NM_005992.1:c.810C= NP_005983.1:p.Phe270=
NM_080646.1:c.810C= NP_542377.1:p.Phe270=
NM_080647.1:c.810C= , LRG_226t1:c.810C= NP_542378.1:p.Phe270=
XM_006724312.1:c.810C= XP_006724375.1:p.Phe270=
XM_011530351.1:c.837C= XP_011528653.1:p.Phe279=
XM_006724312.2:c.810C= XP_006724375.1:p.Phe270=
XM_017028925.1:c.960C= XP_016884414.1:p.Phe320=
XM_017028926.1:c.810C= XP_016884415.1:p.Phe270=
XM_017028927.1:c.111C= XP_016884416.1:p.Phe37=
XM_017028928.1:c.960C= XP_016884417.1:p.Phe320=
NM_001379200.1:c.837C= MANE Select NP_001366129.1:p.Phe279=
NM_080646.2:c.810C= NP_542377.1:p.Phe270=