Canonical Allele Identifier: CA2396032661
Gene: TBX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19766930A= , CM000684.2:g.19766930A= GRCh38
NC_000022.10:g.19754453A= , CM000684.1:g.19754453A= GRCh37
NC_000022.9:g.18134453A= NCBI36
NG_009229.1:g.15228A= , LRG_226:g.15228A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649276.2:c.*63A= MANE Select ENSP00000497003.1:n.*63A=
ENST00000329705.11:c.1009+928A= ENSP00000331176.7:n.1009+928A=
ENST00000332710.8:c.*63A= ENSP00000331791.4:n.*63A=
ENST00000359500.7:c.1009+928A= ENSP00000352483.3:n.1009+928A=
ENST00000621939.1:c.1009+928A= ENSP00000477982.1:n.1009+928A=
NM_005992.1:c.1009+928A= NP_005983.1:n.1009+928A=
NM_080646.1:c.1009+928A= NP_542377.1:n.1009+928A=
NM_080647.1:c.*63A= , LRG_226t1:c.*63A= NP_542378.1:n.*63A=
XM_006724312.1:c.*63A= XP_006724375.1:n.*63A=
XM_011530351.1:c.*63A= XP_011528653.1:n.*63A=
XM_006724312.2:c.*63A= XP_006724375.1:n.*63A=
XM_017028925.1:c.*63A= XP_016884414.1:n.*63A=
XM_017028926.1:c.*63A= XP_016884415.1:n.*63A=
XM_017028927.1:c.*63A= XP_016884416.1:n.*63A=
XM_017028928.1:c.1159+928A= XP_016884417.1:n.1159+928A=
NM_001379200.1:c.*63A= MANE Select NP_001366129.1:n.*63A=
NM_080646.2:c.1009+928A= NP_542377.1:n.1009+928A=