Canonical Allele Identifier: CA2616730162

Gene: DCPS GSEC

Linked Data

• gnomAD v4: 11-126345522-ACCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345523_126345525del , CM000673.2:g.126345523_126345525del	GRCh38
NC_000011.9:g.126215418_126215420del , CM000673.1:g.126215418_126215420del	GRCh37
NC_000011.8:g.125720628_125720630del	NCBI36
NG_053153.1:g.47223_47225del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.924_926del (DCPS) MANE Select	ENSP00000263579.4:p.Pro309del
ENST00000648516.1:c.645_647del (DCPS)	ENSP00000497684.1:p.Pro216del
ENST00000263579.4:c.924_926del (DCPS)	ENSP00000263579.4:p.Pro309del
ENST00000529149.1:n.2274_2276del (DCPS)
ENST00000530860.5:n.435_437del (DCPS)
NM_014026.4:c.924_926del (DCPS)	NP_054745.1:p.Pro309del
NR_033839.1:n.147-3203_147-3201del (GSEC)
XM_011542778.1:c.945_947del (DCPS)	XP_011541080.1:p.Pro316del
XM_011542779.1:c.645_647del (DCPS)	XP_011541081.1:p.Pro216del
XM_011542780.1:c.645_647del (DCPS)	XP_011541082.1:p.Pro216del
NM_001350236.1:c.945_947del (DCPS)	NP_001337165.1:p.Pro316del
NM_014026.5:c.924_926del (DCPS)	NP_054745.1:p.Pro309del
NM_014026.6:c.924_926del (DCPS) MANE Select	NP_054745.1:p.Pro309del
NM_001350236.2:c.945_947del (DCPS)	NP_001337165.1:p.Pro316del