Canonical Allele Identifier: CA1149571883
Gene: PEX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408702_2408706delinsAGCTC , CM000663.2:g.2408702_2408706delinsAGCTC GRCh38
NC_000001.10:g.2340141_2340145delinsAGCTC , CM000663.1:g.2340141_2340145delinsAGCTC GRCh37
NC_000001.9:g.2330001_2330005delinsAGCTC NCBI36
NG_008342.1:g.8866_8870delinsGAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.346_350delinsGAGCT ENSP00000288774.3:p.Glu116=
ENST00000447513.7:c.346_350delinsGAGCT MANE Select ENSP00000407922.2:p.Glu116=
ENST00000650293.1:c.300_304delinsGAGCT
ENST00000288774.7:c.346_350delinsGAGCT ENSP00000288774.3:p.Glu116=
ENST00000447513.6:c.346_350delinsGAGCT ENSP00000407922.2:p.Glu116=
ENST00000502666.1:c.551_555delinsGAGCT ENSP00000461951.1:n.551_555delinsGAGCT
ENST00000507596.5:c.346_350delinsGAGCT ENSP00000424291.1:p.Glu116=
ENST00000508384.5:c.-87_-83delinsGAGCT ENSP00000464289.1:n.-87_-83delinsGAGCT
ENST00000510434.1:c.346_350delinsGAGCT ENSP00000423051.1:p.Glu116=
ENST00000515760.1:n.480_484delinsGAGCT
NM_002617.3:c.346_350delinsGAGCT NP_002608.1:p.Glu116=
NM_153818.1:c.346_350delinsGAGCT NP_722540.1:p.Glu116=
XM_011541573.1:c.346_350delinsGAGCT XP_011539875.1:p.Glu116=
XM_011541574.1:c.-87_-83delinsGAGCT XP_011539876.1:n.-87_-83delinsGAGCT
XM_011541575.1:c.-87_-83delinsGAGCT XP_011539877.1:n.-87_-83delinsGAGCT
XM_011541576.1:c.346_350delinsGAGCT XP_011539878.1:p.Glu116=
XR_946666.1:n.466_470delinsGAGCT
XM_011541576.2:c.346_350delinsGAGCT XP_011539878.1:p.Glu116=
XR_946666.2:n.415_419delinsGAGCT
NM_001374425.1:c.346_350delinsGAGCT NP_001361354.1:p.Glu116=
NM_001374426.1:c.-87_-83delinsGAGCT NP_001361355.1:n.-87_-83delinsGAGCT
NM_001374427.1:c.-87_-83delinsGAGCT NP_001361356.1:n.-87_-83delinsGAGCT
NM_002617.4:c.346_350delinsGAGCT MANE Select NP_002608.1:p.Glu116=
NM_153818.2:c.346_350delinsGAGCT NP_722540.1:p.Glu116=
NR_164636.1:n.465_469delinsGAGCT