Canonical Allele Identifier: CA337984064
Gene: PEX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2406495A>T , CM000663.2:g.2406495A>T GRCh38
NC_000001.10:g.2337934A>T , CM000663.1:g.2337934A>T GRCh37
NC_000001.9:g.2327794A>T NCBI36
NG_008342.1:g.11077T>A
NG_016128.1:g.19721A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.961T>A ENSP00000288774.3:p.Cys321Ser
ENST00000447513.7:c.901T>A MANE Select ENSP00000407922.2:p.Cys301Ser
ENST00000650293.1:c.855T>A
ENST00000288774.7:c.961T>A ENSP00000288774.3:p.Cys321Ser
ENST00000447513.6:c.901T>A ENSP00000407922.2:p.Cys301Ser
ENST00000507596.5:c.901T>A ENSP00000424291.1:p.Cys301Ser
NM_002617.3:c.901T>A NP_002608.1:p.Cys301Ser
NM_153818.1:c.961T>A NP_722540.1:p.Cys321Ser
XM_011541573.1:c.958T>A XP_011539875.1:p.Cys320Ser
XM_011541574.1:c.526T>A XP_011539876.1:p.Cys176Ser
XM_011541575.1:c.526T>A XP_011539877.1:p.Cys176Ser
XR_946666.1:n.1017T>A
XR_946666.2:n.966T>A
NM_001374425.1:c.958T>A NP_001361354.1:p.Cys320Ser
NM_001374426.1:c.526T>A NP_001361355.1:p.Cys176Ser
NM_001374427.1:c.469T>A NP_001361356.1:p.Cys157Ser
NM_002617.4:c.901T>A MANE Select NP_002608.1:p.Cys301Ser
NM_153818.2:c.961T>A NP_722540.1:p.Cys321Ser
NR_164636.1:n.1016T>A