Canonical Allele Identifier: CA410685501
Gene: TBX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19766790G>T , CM000684.2:g.19766790G>T GRCh38
NC_000022.10:g.19754313G>T , CM000684.1:g.19754313G>T GRCh37
NC_000022.9:g.18134313G>T NCBI36
NG_009229.1:g.15088G>T , LRG_226:g.15088G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649276.2:c.1438G>T MANE Select ENSP00000497003.1:p.Ala480Ser
ENST00000329705.11:c.1009+788G>T ENSP00000331176.7:n.1009+788G>T
ENST00000332710.8:c.1411G>T ENSP00000331791.4:p.Ala471Ser
ENST00000359500.7:c.1009+788G>T ENSP00000352483.3:n.1009+788G>T
ENST00000621939.1:c.1009+788G>T ENSP00000477982.1:n.1009+788G>T
NM_005992.1:c.1009+788G>T NP_005983.1:n.1009+788G>T
NM_080646.1:c.1009+788G>T NP_542377.1:n.1009+788G>T
NM_080647.1:c.1411G>T , LRG_226t1:c.1411G>T NP_542378.1:p.Ala471Ser
XM_006724312.1:c.1411G>T XP_006724375.1:p.Ala471Ser
XM_011530351.1:c.1438G>T XP_011528653.1:p.Ala480Ser
XM_006724312.2:c.1411G>T XP_006724375.1:p.Ala471Ser
XM_017028925.1:c.1561G>T XP_016884414.1:p.Ala521Ser
XM_017028926.1:c.1411G>T XP_016884415.1:p.Ala471Ser
XM_017028927.1:c.766G>T XP_016884416.1:p.Ala256Ser
XM_017028928.1:c.1159+788G>T XP_016884417.1:n.1159+788G>T
NM_001379200.1:c.1438G>T MANE Select NP_001366129.1:p.Ala480Ser
NM_080646.2:c.1009+788G>T NP_542377.1:n.1009+788G>T