Canonical Allele Identifier: CA1961433088

Gene: MPPED2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.30486561T>A , CM000673.2:g.30486561T>A	GRCh38
NC_000011.9:g.30508108T>A , CM000673.1:g.30508108T>A	GRCh37
NC_000011.8:g.30464684T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358117.10:c.536+8735A>T MANE Select	ENSP00000350833.4:n.536+8735A>T
ENST00000358117.9:c.536+8735A>T	ENSP00000350833.4:n.536+8735A>T
ENST00000448418.6:c.536+8735A>T	ENSP00000388258.2:n.536+8735A>T
ENST00000525519.1:n.317+8735A>T
ENST00000526437.5:c.*280+8735A>T	ENSP00000432469.1:n.*280+8735A>T
NM_001145399.1:c.536+8735A>T	NP_001138871.1:n.536+8735A>T
NM_001584.2:c.536+8735A>T	NP_001575.1:n.536+8735A>T
XM_005253110.2:c.536+8735A>T	XP_005253167.1:n.536+8735A>T
XM_005253111.2:c.536+8735A>T	XP_005253168.1:n.536+8735A>T
XM_005253112.1:c.536+8735A>T	XP_005253169.1:n.536+8735A>T
XM_005253114.2:c.536+8735A>T	XP_005253171.1:n.536+8735A>T
XM_006718304.2:c.314+8735A>T	XP_006718367.1:n.314+8735A>T
XM_011520345.1:c.314+8735A>T	XP_011518647.1:n.314+8735A>T
XM_011520346.1:c.158+8735A>T	XP_011518648.1:n.158+8735A>T
XM_011520347.1:c.158+8735A>T	XP_011518649.1:n.158+8735A>T
XM_011520348.1:c.158+8735A>T	XP_011518650.1:n.158+8735A>T
XM_005253110.4:c.536+8735A>T	XP_005253167.1:n.536+8735A>T
XM_005253114.4:c.536+8735A>T	XP_005253171.1:n.536+8735A>T
XM_011520347.3:c.158+8735A>T	XP_011518649.1:n.158+8735A>T
XM_017018231.1:c.509+8735A>T	XP_016873720.1:n.509+8735A>T
XM_017018232.2:c.536+8735A>T	XP_016873721.1:n.536+8735A>T
XM_017018233.2:c.314+8735A>T	XP_016873722.1:n.314+8735A>T
XM_017018234.2:c.314+8735A>T	XP_016873723.1:n.314+8735A>T
XM_017018235.2:c.158+8735A>T	XP_016873724.1:n.158+8735A>T
XM_017018236.2:c.158+8735A>T	XP_016873725.1:n.158+8735A>T
XM_017018237.1:c.158+8735A>T	XP_016873726.1:n.158+8735A>T
XM_024448675.1:c.536+8735A>T	XP_024304443.1:n.536+8735A>T
XM_024448676.1:c.536+8735A>T	XP_024304444.1:n.536+8735A>T
NM_001145399.2:c.536+8735A>T	NP_001138871.1:n.536+8735A>T
NM_001145399.3:c.536+8735A>T	NP_001138871.1:n.536+8735A>T
NM_001377952.1:c.536+8735A>T	NP_001364881.1:n.536+8735A>T
NM_001377953.1:c.536+8735A>T	NP_001364882.1:n.536+8735A>T
NM_001377954.1:c.536+8735A>T	NP_001364883.1:n.536+8735A>T
NM_001377955.1:c.536+8735A>T	NP_001364884.1:n.536+8735A>T
NM_001377956.1:c.536+8735A>T	NP_001364885.1:n.536+8735A>T
NM_001584.3:c.536+8735A>T MANE Select	NP_001575.1:n.536+8735A>T
NR_165336.1:n.787+8735A>T
NR_165337.1:n.882+8735A>T
NR_165338.1:n.992+8735A>T
NR_165339.1:n.885+8735A>T
NR_165340.1:n.1104+8735A>T
NR_165341.1:n.743+49433A>T
NR_165342.1:n.1144+8735A>T
NR_165343.1:n.1119+8735A>T
NR_165344.1:n.839+8735A>T
NR_165345.1:n.732+8735A>T
NR_165346.1:n.830+8735A>T
NR_165347.1:n.683+8735A>T
NR_165348.1:n.1067+8735A>T