Canonical Allele Identifier: CA1714331399

Gene: SBDS

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66993289G= , CM000669.2:g.66993289G=	GRCh38
NC_000007.13:g.66458276G= , CM000669.1:g.66458276G=	GRCh37
NC_000007.12:g.66095711G=	NCBI36
NG_007277.1:g.7313C= , LRG_104:g.7313C=
NG_033069.1:g.1485G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.*118C=	ENSP00000394586.1:n.*118C=
ENST00000697860.1:n.354C=
ENST00000697861.1:c.258+923C=	ENSP00000513460.1:n.258+923C=
ENST00000697862.1:c.387C=	ENSP00000513461.1:p.Thr129=
ENST00000697863.1:c.330C=	ENSP00000513462.1:p.Thr110=
ENST00000697864.1:n.1531C=
ENST00000697865.1:c.330C=	ENSP00000513463.1:p.Thr110=
ENST00000697866.1:c.69C=	ENSP00000513464.1:p.Thr23=
ENST00000697867.1:c.227C=
ENST00000697868.1:c.*151C=	ENSP00000513466.1:n.*151C=
ENST00000697869.1:c.*122C=	ENSP00000513467.1:n.*122C=
ENST00000697897.1:c.387C=	ENSP00000513469.1:p.Thr129=
ENST00000246868.7:c.387C= MANE Select	ENSP00000246868.2:p.Thr129=
ENST00000246868.6:c.387C=	ENSP00000246868.2:p.Thr129=
ENST00000414306.5:c.*118C=	ENSP00000394586.1:n.*118C=
ENST00000463579.1:n.276C=
ENST00000490953.5:n.528C=
ENST00000617799.1:c.387C=	ENSP00000483040.1:p.Thr129=
NM_016038.2:c.387C= , LRG_104t1:c.387C=	NP_057122.2:p.Thr129=
NM_016038.3:c.387C=	NP_057122.2:p.Thr129=
NM_016038.4:c.387C= MANE Select	NP_057122.2:p.Thr129=