Canonical Allele Identifier: CA230572966

Gene: DCPS GSEC

Linked Data

• dbSNP Id: rs1028560323
• gnomAD v2: 11-126215493-G-A
• gnomAD v4: 11-126345598-G-A
• MyVariant Identifiers: chr11:g.126215493G>A (hg19) ; chr11:g.126345598G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345598G>A , CM000673.2:g.126345598G>A	GRCh38
NC_000011.9:g.126215493G>A , CM000673.1:g.126215493G>A	GRCh37
NC_000011.8:g.125720703G>A	NCBI36
NG_053153.1:g.47298G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.999G>A (DCPS) MANE Select	ENSP00000263579.4:p.Glu333=
ENST00000648516.1:c.720G>A (DCPS)	ENSP00000497684.1:p.Glu240=
ENST00000263579.4:c.999G>A (DCPS)	ENSP00000263579.4:p.Glu333=
ENST00000529149.1:n.2349G>A (DCPS)
ENST00000530860.5:n.510G>A (DCPS)
NM_014026.4:c.999G>A (DCPS)	NP_054745.1:p.Glu333=
NR_033839.1:n.147-3276C>T (GSEC)
XM_011542778.1:c.1020G>A (DCPS)	XP_011541080.1:p.Glu340=
XM_011542779.1:c.720G>A (DCPS)	XP_011541081.1:p.Glu240=
XM_011542780.1:c.720G>A (DCPS)	XP_011541082.1:p.Glu240=
NM_001350236.1:c.1020G>A (DCPS)	NP_001337165.1:p.Glu340=
NM_014026.5:c.999G>A (DCPS)	NP_054745.1:p.Glu333=
NM_014026.6:c.999G>A (DCPS) MANE Select	NP_054745.1:p.Glu333=
NM_001350236.2:c.1020G>A (DCPS)	NP_001337165.1:p.Glu340=