Canonical Allele Identifier: CA383221195

Gene: DCPS GSEC

Linked Data

• MyVariant Identifiers: chr11:g.126215393A>T (hg19) ; chr11:g.126345498A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345498A>T , CM000673.2:g.126345498A>T	GRCh38
NC_000011.9:g.126215393A>T , CM000673.1:g.126215393A>T	GRCh37
NC_000011.8:g.125720603A>T	NCBI36
NG_053153.1:g.47198A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.899A>T (DCPS) MANE Select	ENSP00000263579.4:p.Glu300Val
ENST00000648516.1:c.620A>T (DCPS)	ENSP00000497684.1:p.Glu207Val
ENST00000263579.4:c.899A>T (DCPS)	ENSP00000263579.4:p.Glu300Val
ENST00000529149.1:n.2249A>T (DCPS)
ENST00000530860.5:n.410A>T (DCPS)
NM_014026.4:c.899A>T (DCPS)	NP_054745.1:p.Glu300Val
NR_033839.1:n.147-3176T>A (GSEC)
XM_011542778.1:c.920A>T (DCPS)	XP_011541080.1:p.Glu307Val
XM_011542779.1:c.620A>T (DCPS)	XP_011541081.1:p.Glu207Val
XM_011542780.1:c.620A>T (DCPS)	XP_011541082.1:p.Glu207Val
NM_001350236.1:c.920A>T (DCPS)	NP_001337165.1:p.Glu307Val
NM_014026.5:c.899A>T (DCPS)	NP_054745.1:p.Glu300Val
NM_014026.6:c.899A>T (DCPS) MANE Select	NP_054745.1:p.Glu300Val
NM_001350236.2:c.920A>T (DCPS)	NP_001337165.1:p.Glu307Val