Canonical Allele Identifier: CA367650556

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66458368C>T (hg19) ; chr7:g.66993381C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66993381C>T , CM000669.2:g.66993381C>T	GRCh38
NC_000007.13:g.66458368C>T , CM000669.1:g.66458368C>T	GRCh37
NC_000007.12:g.66095803C>T	NCBI36
NG_007277.1:g.7221G>A , LRG_104:g.7221G>A
NG_033069.1:g.1577C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.*26G>A	ENSP00000394586.1:n.*26G>A
ENST00000697860.1:n.262G>A
ENST00000697861.1:c.258+831G>A	ENSP00000513460.1:n.258+831G>A
ENST00000697862.1:c.295G>A	ENSP00000513461.1:p.Glu99Lys
ENST00000697863.1:c.238G>A	ENSP00000513462.1:p.Glu80Lys
ENST00000697864.1:n.1439G>A
ENST00000697865.1:c.238G>A	ENSP00000513463.1:p.Glu80Lys
ENST00000697866.1:c.-24G>A	ENSP00000513464.1:n.-24G>A
ENST00000697867.1:c.135G>A
ENST00000697868.1:c.*59G>A	ENSP00000513466.1:n.*59G>A
ENST00000697869.1:c.*30G>A	ENSP00000513467.1:n.*30G>A
ENST00000697897.1:c.295G>A	ENSP00000513469.1:p.Glu99Lys
ENST00000246868.7:c.295G>A MANE Select	ENSP00000246868.2:p.Glu99Lys
ENST00000246868.6:c.295G>A	ENSP00000246868.2:p.Glu99Lys
ENST00000414306.5:c.*26G>A	ENSP00000394586.1:n.*26G>A
ENST00000463579.1:n.184G>A
ENST00000490953.5:n.436G>A
ENST00000617799.1:c.295G>A	ENSP00000483040.1:p.Glu99Lys
NM_016038.2:c.295G>A , LRG_104t1:c.295G>A	NP_057122.2:p.Glu99Lys
NM_016038.3:c.295G>A	NP_057122.2:p.Glu99Lys
NM_016038.4:c.295G>A MANE Select	NP_057122.2:p.Glu99Lys