Canonical Allele Identifier: CA367649841

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66458287T>A (hg19) ; chr7:g.66993300T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66993300T>A , CM000669.2:g.66993300T>A	GRCh38
NC_000007.13:g.66458287T>A , CM000669.1:g.66458287T>A	GRCh37
NC_000007.12:g.66095722T>A	NCBI36
NG_007277.1:g.7302A>T , LRG_104:g.7302A>T
NG_033069.1:g.1496T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.*107A>T	ENSP00000394586.1:n.*107A>T
ENST00000697860.1:n.343A>T
ENST00000697861.1:c.258+912A>T	ENSP00000513460.1:n.258+912A>T
ENST00000697862.1:c.376A>T	ENSP00000513461.1:p.Arg126Ter
ENST00000697863.1:c.319A>T	ENSP00000513462.1:p.Arg107Ter
ENST00000697864.1:n.1520A>T
ENST00000697865.1:c.319A>T	ENSP00000513463.1:p.Arg107Ter
ENST00000697866.1:c.58A>T	ENSP00000513464.1:p.Arg20Ter
ENST00000697867.1:c.216A>T
ENST00000697868.1:c.*140A>T	ENSP00000513466.1:n.*140A>T
ENST00000697869.1:c.*111A>T	ENSP00000513467.1:n.*111A>T
ENST00000697897.1:c.376A>T	ENSP00000513469.1:p.Arg126Ter
ENST00000246868.7:c.376A>T MANE Select	ENSP00000246868.2:p.Arg126Ter
ENST00000246868.6:c.376A>T	ENSP00000246868.2:p.Arg126Ter
ENST00000414306.5:c.*107A>T	ENSP00000394586.1:n.*107A>T
ENST00000463579.1:n.265A>T
ENST00000490953.5:n.517A>T
ENST00000617799.1:c.376A>T	ENSP00000483040.1:p.Arg126Ter
NM_016038.2:c.376A>T , LRG_104t1:c.376A>T	NP_057122.2:p.Arg126Ter
NM_016038.3:c.376A>T	NP_057122.2:p.Arg126Ter
NM_016038.4:c.376A>T MANE Select	NP_057122.2:p.Arg126Ter