Canonical Allele Identifier: CA337986848
Gene: PEX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408462C>T , CM000663.2:g.2408462C>T GRCh38
NC_000001.10:g.2339901C>T , CM000663.1:g.2339901C>T GRCh37
NC_000001.9:g.2329761C>T NCBI36
NG_008342.1:g.9110G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.590G>A ENSP00000288774.3:p.Gly197Glu
ENST00000447513.7:c.590G>A MANE Select ENSP00000407922.2:p.Gly197Glu
ENST00000650293.1:c.544G>A
ENST00000288774.7:c.590G>A ENSP00000288774.3:p.Gly197Glu
ENST00000447513.6:c.590G>A ENSP00000407922.2:p.Gly197Glu
ENST00000507596.5:c.590G>A ENSP00000424291.1:p.Gly197Glu
ENST00000510434.1:c.590G>A ENSP00000423051.1:p.Gly197Glu
NM_002617.3:c.590G>A NP_002608.1:p.Gly197Glu
NM_153818.1:c.590G>A NP_722540.1:p.Gly197Glu
XM_011541573.1:c.590G>A XP_011539875.1:p.Gly197Glu
XM_011541574.1:c.158G>A XP_011539876.1:p.Gly53Glu
XM_011541575.1:c.158G>A XP_011539877.1:p.Gly53Glu
XM_011541576.1:c.590G>A XP_011539878.1:p.Gly197Glu
XR_946666.1:n.710G>A
XM_011541576.2:c.590G>A XP_011539878.1:p.Gly197Glu
XR_946666.2:n.659G>A
NM_001374425.1:c.590G>A NP_001361354.1:p.Gly197Glu
NM_001374426.1:c.158G>A NP_001361355.1:p.Gly53Glu
NM_001374427.1:c.158G>A NP_001361356.1:p.Gly53Glu
NM_002617.4:c.590G>A MANE Select NP_002608.1:p.Gly197Glu
NM_153818.2:c.590G>A NP_722540.1:p.Gly197Glu
NR_164636.1:n.709G>A