Canonical Allele Identifier: CA367647012
Gene: SBDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66991270T>A , CM000669.2:g.66991270T>A GRCh38
NC_000007.13:g.66456257T>A , CM000669.1:g.66456257T>A GRCh37
NC_000007.12:g.66093692T>A NCBI36
NG_007277.1:g.9332A>T , LRG_104:g.9332A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000414306.6:c.*222A>T ENSP00000394586.1:n.*222A>T
ENST00000697860.1:n.458A>T
ENST00000697861.1:c.290A>T ENSP00000513460.1:p.Lys97Ile
ENST00000697862.1:c.460-48A>T ENSP00000513461.1:n.460-48A>T
ENST00000697863.1:c.434A>T ENSP00000513462.1:p.Lys145Ile
ENST00000697864.1:n.1635A>T
ENST00000697865.1:c.434A>T ENSP00000513463.1:p.Lys145Ile
ENST00000697866.1:c.173A>T ENSP00000513464.1:p.Lys58Ile
ENST00000697867.1:c.331A>T
ENST00000697868.1:c.*255A>T ENSP00000513466.1:n.*255A>T
ENST00000697897.1:c.491A>T ENSP00000513469.1:p.Lys164Ile
ENST00000246868.7:c.491A>T MANE Select ENSP00000246868.2:p.Lys164Ile
ENST00000246868.6:c.491A>T ENSP00000246868.2:p.Lys164Ile
ENST00000414306.5:c.*222A>T ENSP00000394586.1:n.*222A>T
ENST00000463579.1:n.380A>T
ENST00000490953.5:n.632A>T
ENST00000617799.1:c.491A>T ENSP00000483040.1:p.Lys164Ile
NM_016038.2:c.491A>T , LRG_104t1:c.491A>T NP_057122.2:p.Lys164Ile
NM_016038.3:c.491A>T NP_057122.2:p.Lys164Ile
NM_016038.4:c.491A>T MANE Select NP_057122.2:p.Lys164Ile