Canonical Allele Identifier: CA410682927
Gene: TBX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19764250G>A , CM000684.2:g.19764250G>A GRCh38
NC_000022.10:g.19751773G>A , CM000684.1:g.19751773G>A GRCh37
NC_000022.9:g.18131773G>A NCBI36
NG_009229.1:g.12548G>A , LRG_226:g.12548G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.161G>A ENSP00000514909.1:p.Gly54Asp
ENST00000649276.2:c.635G>A MANE Select ENSP00000497003.1:p.Gly212Asp
ENST00000680333.1:c.608G>A ENSP00000505472.1:p.Gly203Asp
ENST00000329705.11:c.608G>A ENSP00000331176.7:p.Gly203Asp
ENST00000332710.8:c.608G>A ENSP00000331791.4:p.Gly203Asp
ENST00000359500.7:c.608G>A ENSP00000352483.3:p.Gly203Asp
ENST00000621939.1:c.608G>A ENSP00000477982.1:p.Gly203Asp
NM_005992.1:c.608G>A NP_005983.1:p.Gly203Asp
NM_080646.1:c.608G>A NP_542377.1:p.Gly203Asp
NM_080647.1:c.608G>A , LRG_226t1:c.608G>A NP_542378.1:p.Gly203Asp
XM_006724312.1:c.608G>A XP_006724375.1:p.Gly203Asp
XM_011530351.1:c.635G>A XP_011528653.1:p.Gly212Asp
XM_006724312.2:c.608G>A XP_006724375.1:p.Gly203Asp
XM_017028925.1:c.758G>A XP_016884414.1:p.Gly253Asp
XM_017028926.1:c.608G>A XP_016884415.1:p.Gly203Asp
XM_017028928.1:c.758G>A XP_016884417.1:p.Gly253Asp
NM_001379200.1:c.635G>A MANE Select NP_001366129.1:p.Gly212Asp
NM_080646.2:c.608G>A NP_542377.1:p.Gly203Asp