Canonical Allele Identifier: CA538064
Gene: PEX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2406793_2406804del , CM000663.2:g.2406793_2406804del GRCh38
NC_000001.10:g.2338232_2338243del , CM000663.1:g.2338232_2338243del GRCh37
NC_000001.9:g.2328092_2328103del NCBI36
NG_008342.1:g.10768_10779del
NG_016128.1:g.20019_20030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.752_763del ENSP00000288774.3:p.Ser251Ter
ENST00000447513.7:c.692_703del MANE Select ENSP00000407922.2:p.Ser231Ter
ENST00000650293.1:c.646_657del
ENST00000288774.7:c.752_763del ENSP00000288774.3:p.Ser251Ter
ENST00000447513.6:c.692_703del ENSP00000407922.2:p.Ser231Ter
ENST00000507596.5:c.692_703del ENSP00000424291.1:p.Ser231Ter
ENST00000510434.1:c.*58_*69del ENSP00000423051.1:n.*58_*69del
NM_002617.3:c.692_703del NP_002608.1:p.Ser231Ter
NM_153818.1:c.752_763del NP_722540.1:p.Ser251Ter
XM_011541573.1:c.749_760del XP_011539875.1:p.Ser250Ter
XM_011541574.1:c.317_328del XP_011539876.1:p.Ser106Ter
XM_011541575.1:c.317_328del XP_011539877.1:p.Ser106Ter
XR_946666.1:n.808_819del
XR_946666.2:n.757_768del
NM_001374425.1:c.749_760del NP_001361354.1:p.Ser250Ter
NM_001374426.1:c.317_328del NP_001361355.1:p.Ser106Ter
NM_001374427.1:c.260_271del NP_001361356.1:p.Ser87Ter
NM_002617.4:c.692_703del MANE Select NP_002608.1:p.Ser231Ter
NM_153818.2:c.752_763del NP_722540.1:p.Ser251Ter
NR_164636.1:n.807_818del