Canonical Allele Identifier: CA2007047247

Gene: DCPS GSEC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345537A= , CM000673.2:g.126345537A=	GRCh38
NC_000011.9:g.126215432A= , CM000673.1:g.126215432A=	GRCh37
NC_000011.8:g.125720642A=	NCBI36
NG_053153.1:g.47237A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.938A= (DCPS) MANE Select	ENSP00000263579.4:p.Gln313=
ENST00000648516.1:c.659A= (DCPS)	ENSP00000497684.1:p.Gln220=
ENST00000263579.4:c.938A= (DCPS)	ENSP00000263579.4:p.Gln313=
ENST00000529149.1:n.2288A= (DCPS)
ENST00000530860.5:n.449A= (DCPS)
NM_014026.4:c.938A= (DCPS)	NP_054745.1:p.Gln313=
NR_033839.1:n.147-3215T= (GSEC)
XM_011542778.1:c.959A= (DCPS)	XP_011541080.1:p.Gln320=
XM_011542779.1:c.659A= (DCPS)	XP_011541081.1:p.Gln220=
XM_011542780.1:c.659A= (DCPS)	XP_011541082.1:p.Gln220=
NM_001350236.1:c.959A= (DCPS)	NP_001337165.1:p.Gln320=
NM_014026.5:c.938A= (DCPS)	NP_054745.1:p.Gln313=
NM_014026.6:c.938A= (DCPS) MANE Select	NP_054745.1:p.Gln313=
NM_001350236.2:c.959A= (DCPS)	NP_001337165.1:p.Gln320=