Canonical Allele Identifier: CA367649983

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66458308A>C (hg19) ; chr7:g.66993321A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66993321A>C , CM000669.2:g.66993321A>C	GRCh38
NC_000007.13:g.66458308A>C , CM000669.1:g.66458308A>C	GRCh37
NC_000007.12:g.66095743A>C	NCBI36
NG_007277.1:g.7281T>G , LRG_104:g.7281T>G
NG_033069.1:g.1517A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.*86T>G	ENSP00000394586.1:n.*86T>G
ENST00000697860.1:n.322T>G
ENST00000697861.1:c.258+891T>G	ENSP00000513460.1:n.258+891T>G
ENST00000697862.1:c.355T>G	ENSP00000513461.1:p.Cys119Gly
ENST00000697863.1:c.298T>G	ENSP00000513462.1:p.Cys100Gly
ENST00000697864.1:n.1499T>G
ENST00000697865.1:c.298T>G	ENSP00000513463.1:p.Cys100Gly
ENST00000697866.1:c.37T>G	ENSP00000513464.1:p.Cys13Gly
ENST00000697867.1:c.195T>G
ENST00000697868.1:c.*119T>G	ENSP00000513466.1:n.*119T>G
ENST00000697869.1:c.*90T>G	ENSP00000513467.1:n.*90T>G
ENST00000697897.1:c.355T>G	ENSP00000513469.1:p.Cys119Gly
ENST00000246868.7:c.355T>G MANE Select	ENSP00000246868.2:p.Cys119Gly
ENST00000246868.6:c.355T>G	ENSP00000246868.2:p.Cys119Gly
ENST00000414306.5:c.*86T>G	ENSP00000394586.1:n.*86T>G
ENST00000463579.1:n.244T>G
ENST00000490953.5:n.496T>G
ENST00000617799.1:c.355T>G	ENSP00000483040.1:p.Cys119Gly
NM_016038.2:c.355T>G , LRG_104t1:c.355T>G	NP_057122.2:p.Cys119Gly
NM_016038.3:c.355T>G	NP_057122.2:p.Cys119Gly
NM_016038.4:c.355T>G MANE Select	NP_057122.2:p.Cys119Gly