Canonical Allele Identifier: CA2007047442

Gene: DCPS GSEC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345632G= , CM000673.2:g.126345632G=	GRCh38
NC_000011.9:g.126215527G= , CM000673.1:g.126215527G=	GRCh37
NC_000011.8:g.125720737G=	NCBI36
NG_053153.1:g.47332G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.*19G= (DCPS) MANE Select	ENSP00000263579.4:n.*19G=
ENST00000648516.1:c.*19G= (DCPS)	ENSP00000497684.1:n.*19G=
ENST00000263579.4:c.*19G= (DCPS)	ENSP00000263579.4:n.*19G=
ENST00000529149.1:n.2383G= (DCPS)
ENST00000530860.5:n.544G= (DCPS)
NM_014026.4:c.*19G= (DCPS)	NP_054745.1:n.*19G=
NR_033839.1:n.147-3310C= (GSEC)
XM_011542778.1:c.*19G= (DCPS)	XP_011541080.1:n.*19G=
XM_011542779.1:c.*19G= (DCPS)	XP_011541081.1:n.*19G=
XM_011542780.1:c.*19G= (DCPS)	XP_011541082.1:n.*19G=
NM_001350236.1:c.*19G= (DCPS)	NP_001337165.1:n.*19G=
NM_014026.5:c.*19G= (DCPS)	NP_054745.1:n.*19G=
NM_014026.6:c.*19G= (DCPS) MANE Select	NP_054745.1:n.*19G=
NM_001350236.2:c.*19G= (DCPS)	NP_001337165.1:n.*19G=