Canonical Allele Identifier: CA337987811
Gene: PEX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408613G>A , CM000663.2:g.2408613G>A GRCh38
NC_000001.10:g.2340052G>A , CM000663.1:g.2340052G>A GRCh37
NC_000001.9:g.2329912G>A NCBI36
NG_008342.1:g.8959C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.439C>T ENSP00000288774.3:p.His147Tyr
ENST00000447513.7:c.439C>T MANE Select ENSP00000407922.2:p.His147Tyr
ENST00000650293.1:c.393C>T
ENST00000288774.7:c.439C>T ENSP00000288774.3:p.His147Tyr
ENST00000447513.6:c.439C>T ENSP00000407922.2:p.His147Tyr
ENST00000502666.1:c.644C>T ENSP00000461951.1:n.644C>T
ENST00000507596.5:c.439C>T ENSP00000424291.1:p.His147Tyr
ENST00000508384.5:c.7C>T ENSP00000464289.1:p.His3Tyr
ENST00000510434.1:c.439C>T ENSP00000423051.1:p.His147Tyr
ENST00000515760.1:n.573C>T
NM_002617.3:c.439C>T NP_002608.1:p.His147Tyr
NM_153818.1:c.439C>T NP_722540.1:p.His147Tyr
XM_011541573.1:c.439C>T XP_011539875.1:p.His147Tyr
XM_011541574.1:c.7C>T XP_011539876.1:p.His3Tyr
XM_011541575.1:c.7C>T XP_011539877.1:p.His3Tyr
XM_011541576.1:c.439C>T XP_011539878.1:p.His147Tyr
XR_946666.1:n.559C>T
XM_011541576.2:c.439C>T XP_011539878.1:p.His147Tyr
XR_946666.2:n.508C>T
NM_001374425.1:c.439C>T NP_001361354.1:p.His147Tyr
NM_001374426.1:c.7C>T NP_001361355.1:p.His3Tyr
NM_001374427.1:c.7C>T NP_001361356.1:p.His3Tyr
NM_002617.4:c.439C>T MANE Select NP_002608.1:p.His147Tyr
NM_153818.2:c.439C>T NP_722540.1:p.His147Tyr
NR_164636.1:n.558C>T