Canonical Allele Identifier: CA337988631
Gene: PEX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408738A>C , CM000663.2:g.2408738A>C GRCh38
NC_000001.10:g.2340177A>C , CM000663.1:g.2340177A>C GRCh37
NC_000001.9:g.2330037A>C NCBI36
NG_008342.1:g.8834T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.314T>G ENSP00000288774.3:p.Leu105Arg
ENST00000447513.7:c.314T>G MANE Select ENSP00000407922.2:p.Leu105Arg
ENST00000650293.1:c.268T>G
ENST00000288774.7:c.314T>G ENSP00000288774.3:p.Leu105Arg
ENST00000447513.6:c.314T>G ENSP00000407922.2:p.Leu105Arg
ENST00000502666.1:c.519T>G ENSP00000461951.1:n.519T>G
ENST00000507596.5:c.314T>G ENSP00000424291.1:p.Leu105Arg
ENST00000508384.5:c.-119T>G ENSP00000464289.1:n.-119T>G
ENST00000510434.1:c.314T>G ENSP00000423051.1:p.Leu105Arg
ENST00000515760.1:n.448T>G
NM_002617.3:c.314T>G NP_002608.1:p.Leu105Arg
NM_153818.1:c.314T>G NP_722540.1:p.Leu105Arg
XM_011541573.1:c.314T>G XP_011539875.1:p.Leu105Arg
XM_011541574.1:c.-119T>G XP_011539876.1:n.-119T>G
XM_011541575.1:c.-119T>G XP_011539877.1:n.-119T>G
XM_011541576.1:c.314T>G XP_011539878.1:p.Leu105Arg
XR_946666.1:n.434T>G
XM_011541576.2:c.314T>G XP_011539878.1:p.Leu105Arg
XR_946666.2:n.383T>G
NM_001374425.1:c.314T>G NP_001361354.1:p.Leu105Arg
NM_001374426.1:c.-119T>G NP_001361355.1:n.-119T>G
NM_001374427.1:c.-119T>G NP_001361356.1:n.-119T>G
NM_002617.4:c.314T>G MANE Select NP_002608.1:p.Leu105Arg
NM_153818.2:c.314T>G NP_722540.1:p.Leu105Arg
NR_164636.1:n.433T>G