Canonical Allele Identifier: CA2007047198

Gene: DCPS GSEC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345492T= , CM000673.2:g.126345492T=	GRCh38
NC_000011.9:g.126215387T= , CM000673.1:g.126215387T=	GRCh37
NC_000011.8:g.125720597T=	NCBI36
NG_053153.1:g.47192T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.893T= (DCPS) MANE Select	ENSP00000263579.4:p.Leu298=
ENST00000648516.1:c.614T= (DCPS)	ENSP00000497684.1:p.Leu205=
ENST00000263579.4:c.893T= (DCPS)	ENSP00000263579.4:p.Leu298=
ENST00000529149.1:n.2243T= (DCPS)
ENST00000530860.5:n.404T= (DCPS)
NM_014026.4:c.893T= (DCPS)	NP_054745.1:p.Leu298=
NR_033839.1:n.147-3170A= (GSEC)
XM_011542778.1:c.914T= (DCPS)	XP_011541080.1:p.Leu305=
XM_011542779.1:c.614T= (DCPS)	XP_011541081.1:p.Leu205=
XM_011542780.1:c.614T= (DCPS)	XP_011541082.1:p.Leu205=
NM_001350236.1:c.914T= (DCPS)	NP_001337165.1:p.Leu305=
NM_014026.5:c.893T= (DCPS)	NP_054745.1:p.Leu298=
NM_014026.6:c.893T= (DCPS) MANE Select	NP_054745.1:p.Leu298=
NM_001350236.2:c.914T= (DCPS)	NP_001337165.1:p.Leu305=