Canonical Allele Identifier: CA1714333880

Gene: SBDS TYW1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66995278G= , CM000669.2:g.66995278G=	GRCh38
NC_000007.13:g.66460265G= , CM000669.1:g.66460265G=	GRCh37
NC_000007.12:g.66097700G=	NCBI36
NG_007277.1:g.5324C= , LRG_104:g.5324C=
NG_033069.1:g.3474G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.128+12C= (SBDS)	ENSP00000394586.1:n.128+12C=
ENST00000697861.1:c.128+12C= (SBDS)	ENSP00000513460.1:n.128+12C=
ENST00000697862.1:c.128+12C= (SBDS)	ENSP00000513461.1:n.128+12C=
ENST00000697863.1:c.71+12C= (SBDS)	ENSP00000513462.1:n.71+12C=
ENST00000697864.1:n.336C= (SBDS)
ENST00000697865.1:c.71+12C= (SBDS)	ENSP00000513463.1:n.71+12C=
ENST00000697866.1:c.-371C= (SBDS)	ENSP00000513464.1:n.-371C=
ENST00000697868.1:c.128+12C= (SBDS)	ENSP00000513466.1:n.128+12C=
ENST00000697869.1:c.128+12C= (SBDS)	ENSP00000513467.1:n.128+12C=
ENST00000697897.1:c.128+12C= (SBDS)	ENSP00000513469.1:n.128+12C=
ENST00000246868.7:c.128+12C= (SBDS) MANE Select	ENSP00000246868.2:n.128+12C=
ENST00000246868.6:c.128+12C= (SBDS)	ENSP00000246868.2:n.128+12C=
ENST00000414306.5:c.128+12C= (SBDS)	ENSP00000394586.1:n.128+12C=
ENST00000490953.5:n.277+12C= (SBDS)
ENST00000491969.5:n.106G= (TYW1)
ENST00000617799.1:c.127+12C= (SBDS)	ENSP00000483040.1:n.127+12C=
NM_016038.2:c.128+12C= , LRG_104t1:c.128+12C= (SBDS)	NP_057122.2:n.128+12C=
NM_016038.3:c.128+12C= (SBDS)	NP_057122.2:n.128+12C=
NM_016038.4:c.128+12C= (SBDS) MANE Select	NP_057122.2:n.128+12C=