Canonical Allele Identifier: CA2396032431
Gene: TBX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19766632A= , CM000684.2:g.19766632A= GRCh38
NC_000022.10:g.19754155A= , CM000684.1:g.19754155A= GRCh37
NC_000022.9:g.18134155A= NCBI36
NG_009229.1:g.14930A= , LRG_226:g.14930A=

Transcript Alleles

HGVS Amino-acid change
ENST00000649276.2:c.1280A= MANE Select ENSP00000497003.1:p.Tyr427=
ENST00000329705.11:c.1009+630A= ENSP00000331176.7:n.1009+630A=
ENST00000332710.8:c.1253A= ENSP00000331791.4:p.Tyr418=
ENST00000359500.7:c.1009+630A= ENSP00000352483.3:n.1009+630A=
ENST00000621939.1:c.1009+630A= ENSP00000477982.1:n.1009+630A=
NM_005992.1:c.1009+630A= NP_005983.1:n.1009+630A=
NM_080646.1:c.1009+630A= NP_542377.1:n.1009+630A=
NM_080647.1:c.1253A= , LRG_226t1:c.1253A= NP_542378.1:p.Tyr418=
XM_006724312.1:c.1253A= XP_006724375.1:p.Tyr418=
XM_011530351.1:c.1280A= XP_011528653.1:p.Tyr427=
XM_006724312.2:c.1253A= XP_006724375.1:p.Tyr418=
XM_017028925.1:c.1403A= XP_016884414.1:p.Tyr468=
XM_017028926.1:c.1253A= XP_016884415.1:p.Tyr418=
XM_017028927.1:c.608A= XP_016884416.1:p.Tyr203=
XM_017028928.1:c.1159+630A= XP_016884417.1:n.1159+630A=
NM_001379200.1:c.1280A= MANE Select NP_001366129.1:p.Tyr427=
NM_080646.2:c.1009+630A= NP_542377.1:n.1009+630A=