Canonical Allele Identifier: CA367643998

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66453371T>A (hg19) ; chr7:g.66988384T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66988384T>A , CM000669.2:g.66988384T>A	GRCh38
NC_000007.13:g.66453371T>A , CM000669.1:g.66453371T>A	GRCh37
NC_000007.12:g.66090806T>A	NCBI36
NG_007277.1:g.12218A>T , LRG_104:g.12218A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000414306.6:c.*471A>T	ENSP00000394586.1:n.*471A>T
ENST00000697860.1:n.707A>T
ENST00000697861.1:c.539A>T	ENSP00000513460.1:p.Glu180Val
ENST00000697862.1:c.*181A>T	ENSP00000513461.1:n.*181A>T
ENST00000697863.1:c.683A>T	ENSP00000513462.1:p.Glu228Val
ENST00000697864.1:n.1884A>T
ENST00000697865.1:c.683A>T	ENSP00000513463.1:p.Glu228Val
ENST00000697866.1:c.422A>T	ENSP00000513464.1:p.Glu141Val
ENST00000697867.1:c.718A>T
ENST00000697868.1:c.*504A>T	ENSP00000513466.1:n.*504A>T
ENST00000697897.1:c.740A>T	ENSP00000513469.1:p.Glu247Val
ENST00000246868.7:c.740A>T MANE Select	ENSP00000246868.2:p.Glu247Val
ENST00000246868.6:c.740A>T	ENSP00000246868.2:p.Glu247Val
ENST00000414306.5:c.*471A>T	ENSP00000394586.1:n.*471A>T
ENST00000617799.1:c.740A>T	ENSP00000483040.1:p.Glu247Val
NM_016038.2:c.740A>T , LRG_104t1:c.740A>T	NP_057122.2:p.Glu247Val
NM_016038.3:c.740A>T	NP_057122.2:p.Glu247Val
NM_016038.4:c.740A>T MANE Select	NP_057122.2:p.Glu247Val