Canonical Allele Identifier: CA1714329471
Gene: SBDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66991265T= , CM000669.2:g.66991265T= GRCh38
NC_000007.13:g.66456252T= , CM000669.1:g.66456252T= GRCh37
NC_000007.12:g.66093687T= NCBI36
NG_007277.1:g.9337A= , LRG_104:g.9337A=

Transcript Alleles

HGVS Amino-acid change
ENST00000414306.6:c.*227A= ENSP00000394586.1:n.*227A=
ENST00000697860.1:n.463A=
ENST00000697861.1:c.295A= ENSP00000513460.1:p.Lys99=
ENST00000697862.1:c.460-43A= ENSP00000513461.1:n.460-43A=
ENST00000697863.1:c.439A= ENSP00000513462.1:p.Lys147=
ENST00000697864.1:n.1640A=
ENST00000697865.1:c.439A= ENSP00000513463.1:p.Lys147=
ENST00000697866.1:c.178A= ENSP00000513464.1:p.Lys60=
ENST00000697867.1:c.336A=
ENST00000697868.1:c.*260A= ENSP00000513466.1:n.*260A=
ENST00000697897.1:c.496A= ENSP00000513469.1:p.Lys166=
ENST00000246868.7:c.496A= MANE Select ENSP00000246868.2:p.Lys166=
ENST00000246868.6:c.496A= ENSP00000246868.2:p.Lys166=
ENST00000414306.5:c.*227A= ENSP00000394586.1:n.*227A=
ENST00000463579.1:n.385A=
ENST00000490953.5:n.637A=
ENST00000617799.1:c.496A= ENSP00000483040.1:p.Lys166=
NM_016038.2:c.496A= , LRG_104t1:c.496A= NP_057122.2:p.Lys166=
NM_016038.3:c.496A= NP_057122.2:p.Lys166=
NM_016038.4:c.496A= MANE Select NP_057122.2:p.Lys166=