Canonical Allele Identifier: CA2007047258

Gene: DCPS GSEC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345543G= , CM000673.2:g.126345543G=	GRCh38
NC_000011.9:g.126215438G= , CM000673.1:g.126215438G=	GRCh37
NC_000011.8:g.125720648G=	NCBI36
NG_053153.1:g.47243G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.944G= (DCPS) MANE Select	ENSP00000263579.4:p.Arg315=
ENST00000648516.1:c.665G= (DCPS)	ENSP00000497684.1:p.Arg222=
ENST00000263579.4:c.944G= (DCPS)	ENSP00000263579.4:p.Arg315=
ENST00000529149.1:n.2294G= (DCPS)
ENST00000530860.5:n.455G= (DCPS)
NM_014026.4:c.944G= (DCPS)	NP_054745.1:p.Arg315=
NR_033839.1:n.147-3221C= (GSEC)
XM_011542778.1:c.965G= (DCPS)	XP_011541080.1:p.Arg322=
XM_011542779.1:c.665G= (DCPS)	XP_011541081.1:p.Arg222=
XM_011542780.1:c.665G= (DCPS)	XP_011541082.1:p.Arg222=
NM_001350236.1:c.965G= (DCPS)	NP_001337165.1:p.Arg322=
NM_014026.5:c.944G= (DCPS)	NP_054745.1:p.Arg315=
NM_014026.6:c.944G= (DCPS) MANE Select	NP_054745.1:p.Arg315=
NM_001350236.2:c.965G= (DCPS)	NP_001337165.1:p.Arg322=