Canonical Allele Identifier: CA383221213

Gene: DCPS GSEC

Linked Data

• MyVariant Identifiers: chr11:g.126215402A>T (hg19) ; chr11:g.126345507A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345507A>T , CM000673.2:g.126345507A>T	GRCh38
NC_000011.9:g.126215402A>T , CM000673.1:g.126215402A>T	GRCh37
NC_000011.8:g.125720612A>T	NCBI36
NG_053153.1:g.47207A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.908A>T (DCPS) MANE Select	ENSP00000263579.4:p.Glu303Val
ENST00000648516.1:c.629A>T (DCPS)	ENSP00000497684.1:p.Glu210Val
ENST00000263579.4:c.908A>T (DCPS)	ENSP00000263579.4:p.Glu303Val
ENST00000529149.1:n.2258A>T (DCPS)
ENST00000530860.5:n.419A>T (DCPS)
NM_014026.4:c.908A>T (DCPS)	NP_054745.1:p.Glu303Val
NR_033839.1:n.147-3185T>A (GSEC)
XM_011542778.1:c.929A>T (DCPS)	XP_011541080.1:p.Glu310Val
XM_011542779.1:c.629A>T (DCPS)	XP_011541081.1:p.Glu210Val
XM_011542780.1:c.629A>T (DCPS)	XP_011541082.1:p.Glu210Val
NM_001350236.1:c.929A>T (DCPS)	NP_001337165.1:p.Glu310Val
NM_014026.5:c.908A>T (DCPS)	NP_054745.1:p.Glu303Val
NM_014026.6:c.908A>T (DCPS) MANE Select	NP_054745.1:p.Glu303Val
NM_001350236.2:c.929A>T (DCPS)	NP_001337165.1:p.Glu310Val