Canonical Allele Identifier: CA337989123
Gene: PEX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408849G>C , CM000663.2:g.2408849G>C GRCh38
NC_000001.10:g.2340288G>C , CM000663.1:g.2340288G>C GRCh37
NC_000001.9:g.2330148G>C NCBI36
NG_008342.1:g.8723C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.203C>G ENSP00000288774.3:p.Thr68Ser
ENST00000447513.7:c.203C>G MANE Select ENSP00000407922.2:p.Thr68Ser
ENST00000650293.1:c.157C>G
ENST00000288774.7:c.203C>G ENSP00000288774.3:p.Thr68Ser
ENST00000447513.6:c.203C>G ENSP00000407922.2:p.Thr68Ser
ENST00000502666.1:c.408C>G ENSP00000461951.1:n.408C>G
ENST00000507596.5:c.203C>G ENSP00000424291.1:p.Thr68Ser
ENST00000508384.5:c.-230C>G ENSP00000464289.1:n.-230C>G
ENST00000510434.1:c.203C>G ENSP00000423051.1:p.Thr68Ser
ENST00000514502.1:c.*220C>G ENSP00000425924.1:n.*220C>G
ENST00000515760.1:n.337C>G
NM_002617.3:c.203C>G NP_002608.1:p.Thr68Ser
NM_153818.1:c.203C>G NP_722540.1:p.Thr68Ser
XM_011541573.1:c.203C>G XP_011539875.1:p.Thr68Ser
XM_011541574.1:c.-230C>G XP_011539876.1:n.-230C>G
XM_011541575.1:c.-230C>G XP_011539877.1:n.-230C>G
XM_011541576.1:c.203C>G XP_011539878.1:p.Thr68Ser
XR_946666.1:n.323C>G
XM_011541576.2:c.203C>G XP_011539878.1:p.Thr68Ser
XR_946666.2:n.272C>G
NM_001374425.1:c.203C>G NP_001361354.1:p.Thr68Ser
NM_001374426.1:c.-230C>G NP_001361355.1:n.-230C>G
NM_001374427.1:c.-230C>G NP_001361356.1:n.-230C>G
NM_002617.4:c.203C>G MANE Select NP_002608.1:p.Thr68Ser
NM_153818.2:c.203C>G NP_722540.1:p.Thr68Ser
NR_164636.1:n.322C>G