Canonical Allele Identifier: CA367647002
Gene: SBDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66991269T>G , CM000669.2:g.66991269T>G GRCh38
NC_000007.13:g.66456256T>G , CM000669.1:g.66456256T>G GRCh37
NC_000007.12:g.66093691T>G NCBI36
NG_007277.1:g.9333A>C , LRG_104:g.9333A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000414306.6:c.*223A>C ENSP00000394586.1:n.*223A>C
ENST00000697860.1:n.459A>C
ENST00000697861.1:c.291A>C ENSP00000513460.1:p.Lys97Asn
ENST00000697862.1:c.460-47A>C ENSP00000513461.1:n.460-47A>C
ENST00000697863.1:c.435A>C ENSP00000513462.1:p.Lys145Asn
ENST00000697864.1:n.1636A>C
ENST00000697865.1:c.435A>C ENSP00000513463.1:p.Lys145Asn
ENST00000697866.1:c.174A>C ENSP00000513464.1:p.Lys58Asn
ENST00000697867.1:c.332A>C
ENST00000697868.1:c.*256A>C ENSP00000513466.1:n.*256A>C
ENST00000697897.1:c.492A>C ENSP00000513469.1:p.Lys164Asn
ENST00000246868.7:c.492A>C MANE Select ENSP00000246868.2:p.Lys164Asn
ENST00000246868.6:c.492A>C ENSP00000246868.2:p.Lys164Asn
ENST00000414306.5:c.*223A>C ENSP00000394586.1:n.*223A>C
ENST00000463579.1:n.381A>C
ENST00000490953.5:n.633A>C
ENST00000617799.1:c.492A>C ENSP00000483040.1:p.Lys164Asn
NM_016038.2:c.492A>C , LRG_104t1:c.492A>C NP_057122.2:p.Lys164Asn
NM_016038.3:c.492A>C NP_057122.2:p.Lys164Asn
NM_016038.4:c.492A>C MANE Select NP_057122.2:p.Lys164Asn