Canonical Allele Identifier: CA1149571889
Gene: PEX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408714_2408715delinsAG , CM000663.2:g.2408714_2408715delinsAG GRCh38
NC_000001.10:g.2340153_2340154delinsAG , CM000663.1:g.2340153_2340154delinsAG GRCh37
NC_000001.9:g.2330013_2330014delinsAG NCBI36
NG_008342.1:g.8857_8858delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.337_338delinsCT ENSP00000288774.3:p.Leu113=
ENST00000447513.7:c.337_338delinsCT MANE Select ENSP00000407922.2:p.Leu113=
ENST00000650293.1:c.291_292delinsCT
ENST00000288774.7:c.337_338delinsCT ENSP00000288774.3:p.Leu113=
ENST00000447513.6:c.337_338delinsCT ENSP00000407922.2:p.Leu113=
ENST00000502666.1:c.542_543delinsCT ENSP00000461951.1:n.542_543delinsCT
ENST00000507596.5:c.337_338delinsCT ENSP00000424291.1:p.Leu113=
ENST00000508384.5:c.-96_-95delinsCT ENSP00000464289.1:n.-96_-95delinsCT
ENST00000510434.1:c.337_338delinsCT ENSP00000423051.1:p.Leu113=
ENST00000515760.1:n.471_472delinsCT
NM_002617.3:c.337_338delinsCT NP_002608.1:p.Leu113=
NM_153818.1:c.337_338delinsCT NP_722540.1:p.Leu113=
XM_011541573.1:c.337_338delinsCT XP_011539875.1:p.Leu113=
XM_011541574.1:c.-96_-95delinsCT XP_011539876.1:n.-96_-95delinsCT
XM_011541575.1:c.-96_-95delinsCT XP_011539877.1:n.-96_-95delinsCT
XM_011541576.1:c.337_338delinsCT XP_011539878.1:p.Leu113=
XR_946666.1:n.457_458delinsCT
XM_011541576.2:c.337_338delinsCT XP_011539878.1:p.Leu113=
XR_946666.2:n.406_407delinsCT
NM_001374425.1:c.337_338delinsCT NP_001361354.1:p.Leu113=
NM_001374426.1:c.-96_-95delinsCT NP_001361355.1:n.-96_-95delinsCT
NM_001374427.1:c.-96_-95delinsCT NP_001361356.1:n.-96_-95delinsCT
NM_002617.4:c.337_338delinsCT MANE Select NP_002608.1:p.Leu113=
NM_153818.2:c.337_338delinsCT NP_722540.1:p.Leu113=
NR_164636.1:n.456_457delinsCT