Canonical Allele Identifier: CA1149571869
Gene: PEX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408676G= , CM000663.2:g.2408676G= GRCh38
NC_000001.10:g.2340115G= , CM000663.1:g.2340115G= GRCh37
NC_000001.9:g.2329975G= NCBI36
NG_008342.1:g.8896C=

Transcript Alleles

HGVS Amino-acid change
ENST00000288774.8:c.376C= ENSP00000288774.3:p.Pro126=
ENST00000447513.7:c.376C= MANE Select ENSP00000407922.2:p.Pro126=
ENST00000650293.1:c.330C=
ENST00000288774.7:c.376C= ENSP00000288774.3:p.Pro126=
ENST00000447513.6:c.376C= ENSP00000407922.2:p.Pro126=
ENST00000502666.1:c.581C= ENSP00000461951.1:n.581C=
ENST00000507596.5:c.376C= ENSP00000424291.1:p.Pro126=
ENST00000508384.5:c.-57C= ENSP00000464289.1:n.-57C=
ENST00000510434.1:c.376C= ENSP00000423051.1:p.Pro126=
ENST00000515760.1:n.510C=
NM_002617.3:c.376C= NP_002608.1:p.Pro126=
NM_153818.1:c.376C= NP_722540.1:p.Pro126=
XM_011541573.1:c.376C= XP_011539875.1:p.Pro126=
XM_011541574.1:c.-57C= XP_011539876.1:n.-57C=
XM_011541575.1:c.-57C= XP_011539877.1:n.-57C=
XM_011541576.1:c.376C= XP_011539878.1:p.Pro126=
XR_946666.1:n.496C=
XM_011541576.2:c.376C= XP_011539878.1:p.Pro126=
XR_946666.2:n.445C=
NM_001374425.1:c.376C= NP_001361354.1:p.Pro126=
NM_001374426.1:c.-57C= NP_001361355.1:n.-57C=
NM_001374427.1:c.-57C= NP_001361356.1:n.-57C=
NM_002617.4:c.376C= MANE Select NP_002608.1:p.Pro126=
NM_153818.2:c.376C= NP_722540.1:p.Pro126=
NR_164636.1:n.495C=