Canonical Allele Identifier: CA1149570904
Gene: PEX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2406697C= , CM000663.2:g.2406697C= GRCh38
NC_000001.10:g.2338136C= , CM000663.1:g.2338136C= GRCh37
NC_000001.9:g.2327996C= NCBI36
NG_008342.1:g.10875G=
NG_016128.1:g.19923C=

Transcript Alleles

HGVS Amino-acid change
ENST00000288774.8:c.836+23G= ENSP00000288774.3:n.836+23G=
ENST00000447513.7:c.776+23G= MANE Select ENSP00000407922.2:n.776+23G=
ENST00000650293.1:c.730+23G=
ENST00000288774.7:c.836+23G= ENSP00000288774.3:n.836+23G=
ENST00000447513.6:c.776+23G= ENSP00000407922.2:n.776+23G=
ENST00000507596.5:c.776+23G= ENSP00000424291.1:n.776+23G=
ENST00000510434.1:c.*142+23G= ENSP00000423051.1:n.*142+23G=
NM_002617.3:c.776+23G= NP_002608.1:n.776+23G=
NM_153818.1:c.836+23G= NP_722540.1:n.836+23G=
XM_011541573.1:c.833+23G= XP_011539875.1:n.833+23G=
XM_011541574.1:c.401+23G= XP_011539876.1:n.401+23G=
XM_011541575.1:c.401+23G= XP_011539877.1:n.401+23G=
XR_946666.1:n.892+23G=
XR_946666.2:n.841+23G=
NM_001374425.1:c.833+23G= NP_001361354.1:n.833+23G=
NM_001374426.1:c.401+23G= NP_001361355.1:n.401+23G=
NM_001374427.1:c.344+23G= NP_001361356.1:n.344+23G=
NM_002617.4:c.776+23G= MANE Select NP_002608.1:n.776+23G=
NM_153818.2:c.836+23G= NP_722540.1:n.836+23G=
NR_164636.1:n.891+23G=