Canonical Allele Identifier: CA383221189

Gene: DCPS GSEC

Linked Data

• MyVariant Identifiers: chr11:g.126215390C>T (hg19) ; chr11:g.126345495C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345495C>T , CM000673.2:g.126345495C>T	GRCh38
NC_000011.9:g.126215390C>T , CM000673.1:g.126215390C>T	GRCh37
NC_000011.8:g.125720600C>T	NCBI36
NG_053153.1:g.47195C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.896C>T (DCPS) MANE Select	ENSP00000263579.4:p.Ala299Val
ENST00000648516.1:c.617C>T (DCPS)	ENSP00000497684.1:p.Ala206Val
ENST00000263579.4:c.896C>T (DCPS)	ENSP00000263579.4:p.Ala299Val
ENST00000529149.1:n.2246C>T (DCPS)
ENST00000530860.5:n.407C>T (DCPS)
NM_014026.4:c.896C>T (DCPS)	NP_054745.1:p.Ala299Val
NR_033839.1:n.147-3173G>A (GSEC)
XM_011542778.1:c.917C>T (DCPS)	XP_011541080.1:p.Ala306Val
XM_011542779.1:c.617C>T (DCPS)	XP_011541081.1:p.Ala206Val
XM_011542780.1:c.617C>T (DCPS)	XP_011541082.1:p.Ala206Val
NM_001350236.1:c.917C>T (DCPS)	NP_001337165.1:p.Ala306Val
NM_014026.5:c.896C>T (DCPS)	NP_054745.1:p.Ala299Val
NM_014026.6:c.896C>T (DCPS) MANE Select	NP_054745.1:p.Ala299Val
NM_001350236.2:c.917C>T (DCPS)	NP_001337165.1:p.Ala306Val