Canonical Allele Identifier: CA337988591
Gene: PEX10 HGNC NCBI

Linked Data

gnomAD v4: 1-2408730-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408730T>C , CM000663.2:g.2408730T>C GRCh38
NC_000001.10:g.2340169T>C , CM000663.1:g.2340169T>C GRCh37
NC_000001.9:g.2330029T>C NCBI36
NG_008342.1:g.8842A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.322A>G ENSP00000288774.3:p.Lys108Glu
ENST00000447513.7:c.322A>G MANE Select ENSP00000407922.2:p.Lys108Glu
ENST00000650293.1:c.276A>G
ENST00000288774.7:c.322A>G ENSP00000288774.3:p.Lys108Glu
ENST00000447513.6:c.322A>G ENSP00000407922.2:p.Lys108Glu
ENST00000502666.1:c.527A>G ENSP00000461951.1:n.527A>G
ENST00000507596.5:c.322A>G ENSP00000424291.1:p.Lys108Glu
ENST00000508384.5:c.-111A>G ENSP00000464289.1:n.-111A>G
ENST00000510434.1:c.322A>G ENSP00000423051.1:p.Lys108Glu
ENST00000515760.1:n.456A>G
NM_002617.3:c.322A>G NP_002608.1:p.Lys108Glu
NM_153818.1:c.322A>G NP_722540.1:p.Lys108Glu
XM_011541573.1:c.322A>G XP_011539875.1:p.Lys108Glu
XM_011541574.1:c.-111A>G XP_011539876.1:n.-111A>G
XM_011541575.1:c.-111A>G XP_011539877.1:n.-111A>G
XM_011541576.1:c.322A>G XP_011539878.1:p.Lys108Glu
XR_946666.1:n.442A>G
XM_011541576.2:c.322A>G XP_011539878.1:p.Lys108Glu
XR_946666.2:n.391A>G
NM_001374425.1:c.322A>G NP_001361354.1:p.Lys108Glu
NM_001374426.1:c.-111A>G NP_001361355.1:n.-111A>G
NM_001374427.1:c.-111A>G NP_001361356.1:n.-111A>G
NM_002617.4:c.322A>G MANE Select NP_002608.1:p.Lys108Glu
NM_153818.2:c.322A>G NP_722540.1:p.Lys108Glu
NR_164636.1:n.441A>G