Canonical Allele Identifier: CA1714331410
Gene: SBDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66993296G= , CM000669.2:g.66993296G= GRCh38
NC_000007.13:g.66458283G= , CM000669.1:g.66458283G= GRCh37
NC_000007.12:g.66095718G= NCBI36
NG_007277.1:g.7306C= , LRG_104:g.7306C=
NG_033069.1:g.1492G=

Transcript Alleles

HGVS Amino-acid change
ENST00000414306.6:c.*111C= ENSP00000394586.1:n.*111C=
ENST00000697860.1:n.347C=
ENST00000697861.1:c.258+916C= ENSP00000513460.1:n.258+916C=
ENST00000697862.1:c.380C= ENSP00000513461.1:p.Pro127=
ENST00000697863.1:c.323C= ENSP00000513462.1:p.Pro108=
ENST00000697864.1:n.1524C=
ENST00000697865.1:c.323C= ENSP00000513463.1:p.Pro108=
ENST00000697866.1:c.62C= ENSP00000513464.1:p.Pro21=
ENST00000697867.1:c.220C=
ENST00000697868.1:c.*144C= ENSP00000513466.1:n.*144C=
ENST00000697869.1:c.*115C= ENSP00000513467.1:n.*115C=
ENST00000697897.1:c.380C= ENSP00000513469.1:p.Pro127=
ENST00000246868.7:c.380C= MANE Select ENSP00000246868.2:p.Pro127=
ENST00000246868.6:c.380C= ENSP00000246868.2:p.Pro127=
ENST00000414306.5:c.*111C= ENSP00000394586.1:n.*111C=
ENST00000463579.1:n.269C=
ENST00000490953.5:n.521C=
ENST00000617799.1:c.380C= ENSP00000483040.1:p.Pro127=
NM_016038.2:c.380C= , LRG_104t1:c.380C= NP_057122.2:p.Pro127=
NM_016038.3:c.380C= NP_057122.2:p.Pro127=
NM_016038.4:c.380C= MANE Select NP_057122.2:p.Pro127=