Canonical Allele Identifier: CA477512363

Gene: DCPS GSEC

Linked Data

• dbSNP Id: rs1951917675
• MyVariant Identifiers: chr11:g.126215475G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345580G>A , CM000673.2:g.126345580G>A	GRCh38
NC_000011.9:g.126215475G>A , CM000673.1:g.126215475G>A	GRCh37
NC_000011.8:g.125720685G>A	NCBI36
NG_053153.1:g.47280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.981G>A (DCPS) MANE Select	ENSP00000263579.4:p.Leu327=
ENST00000648516.1:c.702G>A (DCPS)	ENSP00000497684.1:p.Leu234=
ENST00000263579.4:c.981G>A (DCPS)	ENSP00000263579.4:p.Leu327=
ENST00000529149.1:n.2331G>A (DCPS)
ENST00000530860.5:n.492G>A (DCPS)
NM_014026.4:c.981G>A (DCPS)	NP_054745.1:p.Leu327=
NR_033839.1:n.147-3258C>T (GSEC)
XM_011542778.1:c.1002G>A (DCPS)	XP_011541080.1:p.Leu334=
XM_011542779.1:c.702G>A (DCPS)	XP_011541081.1:p.Leu234=
XM_011542780.1:c.702G>A (DCPS)	XP_011541082.1:p.Leu234=
NM_001350236.1:c.1002G>A (DCPS)	NP_001337165.1:p.Leu334=
NM_014026.5:c.981G>A (DCPS)	NP_054745.1:p.Leu327=
NM_014026.6:c.981G>A (DCPS) MANE Select	NP_054745.1:p.Leu327=
NM_001350236.2:c.1002G>A (DCPS)	NP_001337165.1:p.Leu334=