Canonical Allele Identifier: CA1714369701
Gene: SBDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66988475A= , CM000669.2:g.66988475A= GRCh38
NC_000007.13:g.66453462A= , CM000669.1:g.66453462A= GRCh37
NC_000007.12:g.66090897A= NCBI36
NG_007277.1:g.12127T= , LRG_104:g.12127T=

Transcript Alleles

HGVS Amino-acid change
ENST00000414306.6:c.*380T= ENSP00000394586.1:n.*380T=
ENST00000697860.1:n.616T=
ENST00000697861.1:c.448T= ENSP00000513460.1:p.Phe150=
ENST00000697862.1:c.*90T= ENSP00000513461.1:n.*90T=
ENST00000697863.1:c.592T= ENSP00000513462.1:p.Phe198=
ENST00000697864.1:n.1793T=
ENST00000697865.1:c.592T= ENSP00000513463.1:p.Phe198=
ENST00000697866.1:c.331T= ENSP00000513464.1:p.Phe111=
ENST00000697867.1:c.627T=
ENST00000697868.1:c.*413T= ENSP00000513466.1:n.*413T=
ENST00000697897.1:c.649T= ENSP00000513469.1:p.Phe217=
ENST00000246868.7:c.649T= MANE Select ENSP00000246868.2:p.Phe217=
ENST00000246868.6:c.649T= ENSP00000246868.2:p.Phe217=
ENST00000414306.5:c.*380T= ENSP00000394586.1:n.*380T=
ENST00000617799.1:c.649T= ENSP00000483040.1:p.Phe217=
NM_016038.2:c.649T= , LRG_104t1:c.649T= NP_057122.2:p.Phe217=
NM_016038.3:c.649T= NP_057122.2:p.Phe217=
NM_016038.4:c.649T= MANE Select NP_057122.2:p.Phe217=