Canonical Allele Identifier: CA367644003
Gene: SBDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66988384T>G , CM000669.2:g.66988384T>G GRCh38
NC_000007.13:g.66453371T>G , CM000669.1:g.66453371T>G GRCh37
NC_000007.12:g.66090806T>G NCBI36
NG_007277.1:g.12218A>C , LRG_104:g.12218A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000414306.6:c.*471A>C ENSP00000394586.1:n.*471A>C
ENST00000697860.1:n.707A>C
ENST00000697861.1:c.539A>C ENSP00000513460.1:p.Glu180Ala
ENST00000697862.1:c.*181A>C ENSP00000513461.1:n.*181A>C
ENST00000697863.1:c.683A>C ENSP00000513462.1:p.Glu228Ala
ENST00000697864.1:n.1884A>C
ENST00000697865.1:c.683A>C ENSP00000513463.1:p.Glu228Ala
ENST00000697866.1:c.422A>C ENSP00000513464.1:p.Glu141Ala
ENST00000697867.1:c.718A>C
ENST00000697868.1:c.*504A>C ENSP00000513466.1:n.*504A>C
ENST00000697897.1:c.740A>C ENSP00000513469.1:p.Glu247Ala
ENST00000246868.7:c.740A>C MANE Select ENSP00000246868.2:p.Glu247Ala
ENST00000246868.6:c.740A>C ENSP00000246868.2:p.Glu247Ala
ENST00000414306.5:c.*471A>C ENSP00000394586.1:n.*471A>C
ENST00000617799.1:c.740A>C ENSP00000483040.1:p.Glu247Ala
NM_016038.2:c.740A>C , LRG_104t1:c.740A>C NP_057122.2:p.Glu247Ala
NM_016038.3:c.740A>C NP_057122.2:p.Glu247Ala
NM_016038.4:c.740A>C MANE Select NP_057122.2:p.Glu247Ala