Canonical Allele Identifier: CA410683524
Community Standard Title: NM_001379200.1(TBX1):c.850G>C (p.Ala284Pro)
Gene: TBX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19765096G>C , CM000684.2:g.19765096G>C GRCh38
NC_000022.10:g.19752619G>C , CM000684.1:g.19752619G>C GRCh37
NC_000022.9:g.18132619G>C NCBI36
NG_009229.1:g.13394G>C , LRG_226:g.13394G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001379200.1:c.850G>C MANE Select NP_001366129.1:p.Ala284Pro
ENST00000649276.2:c.850G>C MANE Select ENSP00000497003.1:p.Ala284Pro
NM_005992.1:c.823G>C NP_005983.1:p.Ala275Pro
NM_080646.1:c.823G>C NP_542377.1:p.Ala275Pro
NM_080646.2:c.823G>C NP_542377.1:p.Ala275Pro
NM_080647.1:c.823G>C , LRG_226t1:c.823G>C NP_542378.1:p.Ala275Pro
ENST00000329705.11:c.823G>C ENSP00000331176.7:p.Ala275Pro
ENST00000332710.8:c.823G>C ENSP00000331791.4:p.Ala275Pro
ENST00000359500.7:c.823G>C ENSP00000352483.3:p.Ala275Pro
ENST00000484336.1:n.18G>C
ENST00000621939.1:c.823G>C ENSP00000477982.1:p.Ala275Pro
ENST00000700274.1:c.376G>C ENSP00000514909.1:p.Ala126Pro
XM_006724312.1:c.823G>C XP_006724375.1:p.Ala275Pro
XM_006724312.2:c.823G>C XP_006724375.1:p.Ala275Pro
XM_011530351.1:c.850G>C XP_011528653.1:p.Ala284Pro
XM_017028925.1:c.973G>C XP_016884414.1:p.Ala325Pro
XM_017028926.1:c.823G>C XP_016884415.1:p.Ala275Pro
XM_017028927.1:c.124G>C XP_016884416.1:p.Ala42Pro
XM_017028928.1:c.973G>C XP_016884417.1:p.Ala325Pro