Canonical Allele Identifier: CA477512284

Gene: DCPS GSEC

Linked Data

• MyVariant Identifiers: chr11:g.126215397G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345502G>C , CM000673.2:g.126345502G>C	GRCh38
NC_000011.9:g.126215397G>C , CM000673.1:g.126215397G>C	GRCh37
NC_000011.8:g.125720607G>C	NCBI36
NG_053153.1:g.47202G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.903G>C (DCPS) MANE Select	ENSP00000263579.4:p.Val301=
ENST00000648516.1:c.624G>C (DCPS)	ENSP00000497684.1:p.Val208=
ENST00000263579.4:c.903G>C (DCPS)	ENSP00000263579.4:p.Val301=
ENST00000529149.1:n.2253G>C (DCPS)
ENST00000530860.5:n.414G>C (DCPS)
NM_014026.4:c.903G>C (DCPS)	NP_054745.1:p.Val301=
NR_033839.1:n.147-3180C>G (GSEC)
XM_011542778.1:c.924G>C (DCPS)	XP_011541080.1:p.Val308=
XM_011542779.1:c.624G>C (DCPS)	XP_011541081.1:p.Val208=
XM_011542780.1:c.624G>C (DCPS)	XP_011541082.1:p.Val208=
NM_001350236.1:c.924G>C (DCPS)	NP_001337165.1:p.Val308=
NM_014026.5:c.903G>C (DCPS)	NP_054745.1:p.Val301=
NM_014026.6:c.903G>C (DCPS) MANE Select	NP_054745.1:p.Val301=
NM_001350236.2:c.924G>C (DCPS)	NP_001337165.1:p.Val308=