Canonical Allele Identifier: CA367649957

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66458305C>G (hg19) ; chr7:g.66993318C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66993318C>G , CM000669.2:g.66993318C>G	GRCh38
NC_000007.13:g.66458305C>G , CM000669.1:g.66458305C>G	GRCh37
NC_000007.12:g.66095740C>G	NCBI36
NG_007277.1:g.7284G>C , LRG_104:g.7284G>C
NG_033069.1:g.1514C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.*89G>C	ENSP00000394586.1:n.*89G>C
ENST00000697860.1:n.325G>C
ENST00000697861.1:c.258+894G>C	ENSP00000513460.1:n.258+894G>C
ENST00000697862.1:c.358G>C	ENSP00000513461.1:p.Val120Leu
ENST00000697863.1:c.301G>C	ENSP00000513462.1:p.Val101Leu
ENST00000697864.1:n.1502G>C
ENST00000697865.1:c.301G>C	ENSP00000513463.1:p.Val101Leu
ENST00000697866.1:c.40G>C	ENSP00000513464.1:p.Val14Leu
ENST00000697867.1:c.198G>C
ENST00000697868.1:c.*122G>C	ENSP00000513466.1:n.*122G>C
ENST00000697869.1:c.*93G>C	ENSP00000513467.1:n.*93G>C
ENST00000697897.1:c.358G>C	ENSP00000513469.1:p.Val120Leu
ENST00000246868.7:c.358G>C MANE Select	ENSP00000246868.2:p.Val120Leu
ENST00000246868.6:c.358G>C	ENSP00000246868.2:p.Val120Leu
ENST00000414306.5:c.*89G>C	ENSP00000394586.1:n.*89G>C
ENST00000463579.1:n.247G>C
ENST00000490953.5:n.499G>C
ENST00000617799.1:c.358G>C	ENSP00000483040.1:p.Val120Leu
NM_016038.2:c.358G>C , LRG_104t1:c.358G>C	NP_057122.2:p.Val120Leu
NM_016038.3:c.358G>C	NP_057122.2:p.Val120Leu
NM_016038.4:c.358G>C MANE Select	NP_057122.2:p.Val120Leu