Canonical Allele Identifier: CA537999
Gene: PEX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2406561C>T , CM000663.2:g.2406561C>T GRCh38
NC_000001.10:g.2338000C>T , CM000663.1:g.2338000C>T GRCh37
NC_000001.9:g.2327860C>T NCBI36
NG_008342.1:g.11011G>A
NG_016128.1:g.19787C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.895G>A ENSP00000288774.3:p.Glu299Lys
ENST00000447513.7:c.835G>A MANE Select ENSP00000407922.2:p.Glu279Lys
ENST00000650293.1:c.789G>A
ENST00000288774.7:c.895G>A ENSP00000288774.3:p.Glu299Lys
ENST00000447513.6:c.835G>A ENSP00000407922.2:p.Glu279Lys
ENST00000507596.5:c.835G>A ENSP00000424291.1:p.Glu279Lys
ENST00000510434.1:c.*201G>A ENSP00000423051.1:n.*201G>A
NM_002617.3:c.835G>A NP_002608.1:p.Glu279Lys
NM_153818.1:c.895G>A NP_722540.1:p.Glu299Lys
XM_011541573.1:c.892G>A XP_011539875.1:p.Glu298Lys
XM_011541574.1:c.460G>A XP_011539876.1:p.Glu154Lys
XM_011541575.1:c.460G>A XP_011539877.1:p.Glu154Lys
XR_946666.1:n.951G>A
XR_946666.2:n.900G>A
NM_001374425.1:c.892G>A NP_001361354.1:p.Glu298Lys
NM_001374426.1:c.460G>A NP_001361355.1:p.Glu154Lys
NM_001374427.1:c.403G>A NP_001361356.1:p.Glu135Lys
NM_002617.4:c.835G>A MANE Select NP_002608.1:p.Glu279Lys
NM_153818.2:c.895G>A NP_722540.1:p.Glu299Lys
NR_164636.1:n.950G>A