Canonical Allele Identifier: CA383221205

Gene: DCPS GSEC

Linked Data

• MyVariant Identifiers: chr11:g.126215399T>C (hg19) ; chr11:g.126345504T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126345504T>C , CM000673.2:g.126345504T>C	GRCh38
NC_000011.9:g.126215399T>C , CM000673.1:g.126215399T>C	GRCh37
NC_000011.8:g.125720609T>C	NCBI36
NG_053153.1:g.47204T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263579.5:c.905T>C (DCPS) MANE Select	ENSP00000263579.4:p.Ile302Thr
ENST00000648516.1:c.626T>C (DCPS)	ENSP00000497684.1:p.Ile209Thr
ENST00000263579.4:c.905T>C (DCPS)	ENSP00000263579.4:p.Ile302Thr
ENST00000529149.1:n.2255T>C (DCPS)
ENST00000530860.5:n.416T>C (DCPS)
NM_014026.4:c.905T>C (DCPS)	NP_054745.1:p.Ile302Thr
NR_033839.1:n.147-3182A>G (GSEC)
XM_011542778.1:c.926T>C (DCPS)	XP_011541080.1:p.Ile309Thr
XM_011542779.1:c.626T>C (DCPS)	XP_011541081.1:p.Ile209Thr
XM_011542780.1:c.626T>C (DCPS)	XP_011541082.1:p.Ile209Thr
NM_001350236.1:c.926T>C (DCPS)	NP_001337165.1:p.Ile309Thr
NM_014026.5:c.905T>C (DCPS)	NP_054745.1:p.Ile302Thr
NM_014026.6:c.905T>C (DCPS) MANE Select	NP_054745.1:p.Ile302Thr
NM_001350236.2:c.926T>C (DCPS)	NP_001337165.1:p.Ile309Thr