Canonical Allele Identifier: CA337984211
Gene: PEX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2406520G>C , CM000663.2:g.2406520G>C GRCh38
NC_000001.10:g.2337959G>C , CM000663.1:g.2337959G>C GRCh37
NC_000001.9:g.2327819G>C NCBI36
NG_008342.1:g.11052C>G
NG_016128.1:g.19746G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.936C>G ENSP00000288774.3:p.Phe312Leu
ENST00000447513.7:c.876C>G MANE Select ENSP00000407922.2:p.Phe292Leu
ENST00000650293.1:c.830C>G
ENST00000288774.7:c.936C>G ENSP00000288774.3:p.Phe312Leu
ENST00000447513.6:c.876C>G ENSP00000407922.2:p.Phe292Leu
ENST00000507596.5:c.876C>G ENSP00000424291.1:p.Phe292Leu
ENST00000510434.1:c.*242C>G ENSP00000423051.1:n.*242C>G
NM_002617.3:c.876C>G NP_002608.1:p.Phe292Leu
NM_153818.1:c.936C>G NP_722540.1:p.Phe312Leu
XM_011541573.1:c.933C>G XP_011539875.1:p.Phe311Leu
XM_011541574.1:c.501C>G XP_011539876.1:p.Phe167Leu
XM_011541575.1:c.501C>G XP_011539877.1:p.Phe167Leu
XR_946666.1:n.992C>G
XR_946666.2:n.941C>G
NM_001374425.1:c.933C>G NP_001361354.1:p.Phe311Leu
NM_001374426.1:c.501C>G NP_001361355.1:p.Phe167Leu
NM_001374427.1:c.444C>G NP_001361356.1:p.Phe148Leu
NM_002617.4:c.876C>G MANE Select NP_002608.1:p.Phe292Leu
NM_153818.2:c.936C>G NP_722540.1:p.Phe312Leu
NR_164636.1:n.991C>G