Canonical Allele Identifier: CA410685155
Gene: TBX1 HGNC NCBI

Linked Data

dbSNP Id: rs2145839168

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19766719A>C , CM000684.2:g.19766719A>C GRCh38
NC_000022.10:g.19754242A>C , CM000684.1:g.19754242A>C GRCh37
NC_000022.9:g.18134242A>C NCBI36
NG_009229.1:g.15017A>C , LRG_226:g.15017A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649276.2:c.1367A>C MANE Select ENSP00000497003.1:p.His456Pro
ENST00000329705.11:c.1009+717A>C ENSP00000331176.7:n.1009+717A>C
ENST00000332710.8:c.1340A>C ENSP00000331791.4:p.His447Pro
ENST00000359500.7:c.1009+717A>C ENSP00000352483.3:n.1009+717A>C
ENST00000621939.1:c.1009+717A>C ENSP00000477982.1:n.1009+717A>C
NM_005992.1:c.1009+717A>C NP_005983.1:n.1009+717A>C
NM_080646.1:c.1009+717A>C NP_542377.1:n.1009+717A>C
NM_080647.1:c.1340A>C , LRG_226t1:c.1340A>C NP_542378.1:p.His447Pro
XM_006724312.1:c.1340A>C XP_006724375.1:p.His447Pro
XM_011530351.1:c.1367A>C XP_011528653.1:p.His456Pro
XM_006724312.2:c.1340A>C XP_006724375.1:p.His447Pro
XM_017028925.1:c.1490A>C XP_016884414.1:p.His497Pro
XM_017028926.1:c.1340A>C XP_016884415.1:p.His447Pro
XM_017028927.1:c.695A>C XP_016884416.1:p.His232Pro
XM_017028928.1:c.1159+717A>C XP_016884417.1:n.1159+717A>C
NM_001379200.1:c.1367A>C MANE Select NP_001366129.1:p.His456Pro
NM_080646.2:c.1009+717A>C NP_542377.1:n.1009+717A>C