Canonical Allele Identifier: CA477512265

Gene: DCPS GSEC

Linked Data

• MyVariant Identifiers: chr11:g.126215391T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345496T>G , CM000673.2:g.126345496T>G	GRCh38
NC_000011.9:g.126215391T>G , CM000673.1:g.126215391T>G	GRCh37
NC_000011.8:g.125720601T>G	NCBI36
NG_053153.1:g.47196T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.897T>G (DCPS) MANE Select	ENSP00000263579.4:p.Ala299=
ENST00000648516.1:c.618T>G (DCPS)	ENSP00000497684.1:p.Ala206=
ENST00000263579.4:c.897T>G (DCPS)	ENSP00000263579.4:p.Ala299=
ENST00000529149.1:n.2247T>G (DCPS)
ENST00000530860.5:n.408T>G (DCPS)
NM_014026.4:c.897T>G (DCPS)	NP_054745.1:p.Ala299=
NR_033839.1:n.147-3174A>C (GSEC)
XM_011542778.1:c.918T>G (DCPS)	XP_011541080.1:p.Ala306=
XM_011542779.1:c.618T>G (DCPS)	XP_011541081.1:p.Ala206=
XM_011542780.1:c.618T>G (DCPS)	XP_011541082.1:p.Ala206=
NM_001350236.1:c.918T>G (DCPS)	NP_001337165.1:p.Ala306=
NM_014026.5:c.897T>G (DCPS)	NP_054745.1:p.Ala299=
NM_014026.6:c.897T>G (DCPS) MANE Select	NP_054745.1:p.Ala299=
NM_001350236.2:c.918T>G (DCPS)	NP_001337165.1:p.Ala306=