Canonical Allele Identifier: CA477512302

Gene: DCPS GSEC

Linked Data

• gnomAD v4: 11-126345523-C-T
• MyVariant Identifiers: chr11:g.126215418C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345523C>T , CM000673.2:g.126345523C>T	GRCh38
NC_000011.9:g.126215418C>T , CM000673.1:g.126215418C>T	GRCh37
NC_000011.8:g.125720628C>T	NCBI36
NG_053153.1:g.47223C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.924C>T (DCPS) MANE Select	ENSP00000263579.4:p.Asp308=
ENST00000648516.1:c.645C>T (DCPS)	ENSP00000497684.1:p.Asp215=
ENST00000263579.4:c.924C>T (DCPS)	ENSP00000263579.4:p.Asp308=
ENST00000529149.1:n.2274C>T (DCPS)
ENST00000530860.5:n.435C>T (DCPS)
NM_014026.4:c.924C>T (DCPS)	NP_054745.1:p.Asp308=
NR_033839.1:n.147-3201G>A (GSEC)
XM_011542778.1:c.945C>T (DCPS)	XP_011541080.1:p.Asp315=
XM_011542779.1:c.645C>T (DCPS)	XP_011541081.1:p.Asp215=
XM_011542780.1:c.645C>T (DCPS)	XP_011541082.1:p.Asp215=
NM_001350236.1:c.945C>T (DCPS)	NP_001337165.1:p.Asp315=
NM_014026.5:c.924C>T (DCPS)	NP_054745.1:p.Asp308=
NM_014026.6:c.924C>T (DCPS) MANE Select	NP_054745.1:p.Asp308=
NM_001350236.2:c.945C>T (DCPS)	NP_001337165.1:p.Asp315=