Canonical Allele Identifier: CA1008868845
Gene: MPC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.167933806_167933814del , CM000663.2:g.167933806_167933814del GRCh38
NC_000001.10:g.167903044_167903052del , CM000663.1:g.167903044_167903052del GRCh37
NC_000001.9:g.166169668_166169676del NCBI36
NG_053062.1:g.2568_2576del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271373.9:c.109+1919_109+1927del MANE Select ENSP00000271373.4:n.109+1919_109+1927del
ENST00000271373.8:c.109+1919_109+1927del ENSP00000271373.4:n.109+1919_109+1927del
ENST00000367846.8:c.109+1919_109+1927del ENSP00000356820.4:n.109+1919_109+1927del
ENST00000458574.1:c.109+1919_109+1927del ENSP00000392874.1:n.109+1919_109+1927del
NM_001143674.3:c.109+1919_109+1927del NP_001137146.1:n.109+1919_109+1927del
NM_015415.3:c.109+1919_109+1927del NP_056230.1:n.109+1919_109+1927del
NR_026550.2:n.469+1919_469+1927del
XM_006711266.2:c.109+1919_109+1927del XP_006711329.1:n.109+1919_109+1927del
XM_006711266.3:c.109+1919_109+1927del XP_006711329.1:n.109+1919_109+1927del
NM_001143674.4:c.109+1919_109+1927del MANE Select NP_001137146.1:n.109+1919_109+1927del
NR_026550.3:n.264+1919_264+1927del