Canonical Allele Identifier: CA455780044

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66458282T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66993295T>G , CM000669.2:g.66993295T>G	GRCh38
NC_000007.13:g.66458282T>G , CM000669.1:g.66458282T>G	GRCh37
NC_000007.12:g.66095717T>G	NCBI36
NG_007277.1:g.7307A>C , LRG_104:g.7307A>C
NG_033069.1:g.1491T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.*112A>C	ENSP00000394586.1:n.*112A>C
ENST00000697860.1:n.348A>C
ENST00000697861.1:c.258+917A>C	ENSP00000513460.1:n.258+917A>C
ENST00000697862.1:c.381A>C	ENSP00000513461.1:p.Pro127=
ENST00000697863.1:c.324A>C	ENSP00000513462.1:p.Pro108=
ENST00000697864.1:n.1525A>C
ENST00000697865.1:c.324A>C	ENSP00000513463.1:p.Pro108=
ENST00000697866.1:c.63A>C	ENSP00000513464.1:p.Pro21=
ENST00000697867.1:c.221A>C
ENST00000697868.1:c.*145A>C	ENSP00000513466.1:n.*145A>C
ENST00000697869.1:c.*116A>C	ENSP00000513467.1:n.*116A>C
ENST00000697897.1:c.381A>C	ENSP00000513469.1:p.Pro127=
ENST00000246868.7:c.381A>C MANE Select	ENSP00000246868.2:p.Pro127=
ENST00000246868.6:c.381A>C	ENSP00000246868.2:p.Pro127=
ENST00000414306.5:c.*112A>C	ENSP00000394586.1:n.*112A>C
ENST00000463579.1:n.270A>C
ENST00000490953.5:n.522A>C
ENST00000617799.1:c.381A>C	ENSP00000483040.1:p.Pro127=
NM_016038.2:c.381A>C , LRG_104t1:c.381A>C	NP_057122.2:p.Pro127=
NM_016038.3:c.381A>C	NP_057122.2:p.Pro127=
NM_016038.4:c.381A>C MANE Select	NP_057122.2:p.Pro127=