Canonical Allele Identifier: CA337989060
Gene: PEX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408828C>T , CM000663.2:g.2408828C>T GRCh38
NC_000001.10:g.2340267C>T , CM000663.1:g.2340267C>T GRCh37
NC_000001.9:g.2330127C>T NCBI36
NG_008342.1:g.8744G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.224G>A ENSP00000288774.3:p.Ser75Asn
ENST00000447513.7:c.224G>A MANE Select ENSP00000407922.2:p.Ser75Asn
ENST00000650293.1:c.178G>A
ENST00000288774.7:c.224G>A ENSP00000288774.3:p.Ser75Asn
ENST00000447513.6:c.224G>A ENSP00000407922.2:p.Ser75Asn
ENST00000502666.1:c.429G>A ENSP00000461951.1:n.429G>A
ENST00000507596.5:c.224G>A ENSP00000424291.1:p.Ser75Asn
ENST00000508384.5:c.-209G>A ENSP00000464289.1:n.-209G>A
ENST00000510434.1:c.224G>A ENSP00000423051.1:p.Ser75Asn
ENST00000514502.1:c.*241G>A ENSP00000425924.1:n.*241G>A
ENST00000515760.1:n.358G>A
NM_002617.3:c.224G>A NP_002608.1:p.Ser75Asn
NM_153818.1:c.224G>A NP_722540.1:p.Ser75Asn
XM_011541573.1:c.224G>A XP_011539875.1:p.Ser75Asn
XM_011541574.1:c.-209G>A XP_011539876.1:n.-209G>A
XM_011541575.1:c.-209G>A XP_011539877.1:n.-209G>A
XM_011541576.1:c.224G>A XP_011539878.1:p.Ser75Asn
XR_946666.1:n.344G>A
XM_011541576.2:c.224G>A XP_011539878.1:p.Ser75Asn
XR_946666.2:n.293G>A
NM_001374425.1:c.224G>A NP_001361354.1:p.Ser75Asn
NM_001374426.1:c.-209G>A NP_001361355.1:n.-209G>A
NM_001374427.1:c.-209G>A NP_001361356.1:n.-209G>A
NM_002617.4:c.224G>A MANE Select NP_002608.1:p.Ser75Asn
NM_153818.2:c.224G>A NP_722540.1:p.Ser75Asn
NR_164636.1:n.343G>A