Canonical Allele Identifier: CA2616730158

Gene: DCPS GSEC

Linked Data

• gnomAD v4: 11-126345511-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345513del , CM000673.2:g.126345513del	GRCh38
NC_000011.9:g.126215408del , CM000673.1:g.126215408del	GRCh37
NC_000011.8:g.125720618del	NCBI36
NG_053153.1:g.47213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.914del (DCPS) MANE Select	ENSP00000263579.4:p.Leu305TrpfsTer?
ENST00000648516.1:c.635del (DCPS)	ENSP00000497684.1:p.Leu212TrpfsTer?
ENST00000263579.4:c.914del (DCPS)	ENSP00000263579.4:p.Leu305TrpfsTer?
ENST00000529149.1:n.2264del (DCPS)
ENST00000530860.5:n.425del (DCPS)
NM_014026.4:c.914del (DCPS)	NP_054745.1:p.Leu305TrpfsTer?
NR_033839.1:n.147-3190del (GSEC)
XM_011542778.1:c.935del (DCPS)	XP_011541080.1:p.Leu312TrpfsTer?
XM_011542779.1:c.635del (DCPS)	XP_011541081.1:p.Leu212TrpfsTer?
XM_011542780.1:c.635del (DCPS)	XP_011541082.1:p.Leu212TrpfsTer?
NM_001350236.1:c.935del (DCPS)	NP_001337165.1:p.Leu312TrpfsTer?
NM_014026.5:c.914del (DCPS)	NP_054745.1:p.Leu305TrpfsTer?
NM_014026.6:c.914del (DCPS) MANE Select	NP_054745.1:p.Leu305TrpfsTer?
NM_001350236.2:c.935del (DCPS)	NP_001337165.1:p.Leu312TrpfsTer?