Canonical Allele Identifier: CA645559382

Gene: SBDS

Linked Data

• gnomAD v4: 7-66993419-TA-T
• COSMIC: COSM5513942

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66993426del , CM000669.2:g.66993426del	GRCh38
NC_000007.13:g.66458413del , CM000669.1:g.66458413del	GRCh37
NC_000007.12:g.66095848del	NCBI36
NG_007277.1:g.7182del , LRG_104:g.7182del
NG_033069.1:g.1622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.251-3del	ENSP00000394586.1:n.251-3del
ENST00000697860.1:n.226-3del
ENST00000697861.1:c.258+792del	ENSP00000513460.1:n.258+792del
ENST00000697862.1:c.259-3del	ENSP00000513461.1:n.259-3del
ENST00000697863.1:c.202-3del	ENSP00000513462.1:n.202-3del
ENST00000697864.1:n.1403-3del
ENST00000697865.1:c.202-3del	ENSP00000513463.1:n.202-3del
ENST00000697866.1:c.-60-3del	ENSP00000513464.1:n.-60-3del
ENST00000697867.1:c.99-3del
ENST00000697868.1:c.*23-3del	ENSP00000513466.1:n.*23-3del
ENST00000697869.1:c.195-3del	ENSP00000513467.1:n.195-3del
ENST00000697897.1:c.259-3del	ENSP00000513469.1:n.259-3del
ENST00000246868.7:c.259-3del MANE Select	ENSP00000246868.2:n.259-3del
ENST00000246868.6:c.259-3del	ENSP00000246868.2:n.259-3del
ENST00000414306.5:c.251-3del	ENSP00000394586.1:n.251-3del
ENST00000463579.1:n.148-3del
ENST00000490953.5:n.400-3del
ENST00000617799.1:c.259-3del	ENSP00000483040.1:n.259-3del
NM_016038.2:c.259-3del , LRG_104t1:c.259-3del	NP_057122.2:n.259-3del
NM_016038.3:c.259-3del	NP_057122.2:n.259-3del
NM_016038.4:c.259-3del MANE Select	NP_057122.2:n.259-3del