Canonical Allele Identifier: CA2007047264

Gene: DCPS GSEC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345545A= , CM000673.2:g.126345545A=	GRCh38
NC_000011.9:g.126215440A= , CM000673.1:g.126215440A=	GRCh37
NC_000011.8:g.125720650A=	NCBI36
NG_053153.1:g.47245A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.946A= (DCPS) MANE Select	ENSP00000263579.4:p.Thr316=
ENST00000648516.1:c.667A= (DCPS)	ENSP00000497684.1:p.Thr223=
ENST00000263579.4:c.946A= (DCPS)	ENSP00000263579.4:p.Thr316=
ENST00000529149.1:n.2296A= (DCPS)
ENST00000530860.5:n.457A= (DCPS)
NM_014026.4:c.946A= (DCPS)	NP_054745.1:p.Thr316=
NR_033839.1:n.147-3223T= (GSEC)
XM_011542778.1:c.967A= (DCPS)	XP_011541080.1:p.Thr323=
XM_011542779.1:c.667A= (DCPS)	XP_011541081.1:p.Thr223=
XM_011542780.1:c.667A= (DCPS)	XP_011541082.1:p.Thr223=
NM_001350236.1:c.967A= (DCPS)	NP_001337165.1:p.Thr323=
NM_014026.5:c.946A= (DCPS)	NP_054745.1:p.Thr316=
NM_014026.6:c.946A= (DCPS) MANE Select	NP_054745.1:p.Thr316=
NM_001350236.2:c.967A= (DCPS)	NP_001337165.1:p.Thr323=