Canonical Allele Identifier: CA1149571807
Gene: PEX10 HGNC NCBI

Linked Data

dbSNP Id: rs1643082652

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408536_2408544del , CM000663.2:g.2408536_2408544del GRCh38
NC_000001.10:g.2339975_2339983del , CM000663.1:g.2339975_2339983del GRCh37
NC_000001.9:g.2329835_2329843del NCBI36
NG_008342.1:g.9028_9036del

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.508_516del ENSP00000288774.3:p.Gly170_Ala172del
ENST00000447513.7:c.508_516del MANE Select ENSP00000407922.2:p.Gly170_Ala172del
ENST00000650293.1:c.462_470del
ENST00000288774.7:c.508_516del ENSP00000288774.3:p.Gly170_Ala172del
ENST00000447513.6:c.508_516del ENSP00000407922.2:p.Gly170_Ala172del
ENST00000507596.5:c.508_516del ENSP00000424291.1:p.Gly170_Ala172del
ENST00000508384.5:c.76_84del ENSP00000464289.1:p.Gly26_Ala28del
ENST00000510434.1:c.508_516del ENSP00000423051.1:p.Gly170_Ala172del
NM_002617.3:c.508_516del NP_002608.1:p.Gly170_Ala172del
NM_153818.1:c.508_516del NP_722540.1:p.Gly170_Ala172del
XM_011541573.1:c.508_516del XP_011539875.1:p.Gly170_Ala172del
XM_011541574.1:c.76_84del XP_011539876.1:p.Gly26_Ala28del
XM_011541575.1:c.76_84del XP_011539877.1:p.Gly26_Ala28del
XM_011541576.1:c.508_516del XP_011539878.1:p.Gly170_Ala172del
XR_946666.1:n.628_636del
XM_011541576.2:c.508_516del XP_011539878.1:p.Gly170_Ala172del
XR_946666.2:n.577_585del
NM_001374425.1:c.508_516del NP_001361354.1:p.Gly170_Ala172del
NM_001374426.1:c.76_84del NP_001361355.1:p.Gly26_Ala28del
NM_001374427.1:c.76_84del NP_001361356.1:p.Gly26_Ala28del
NM_002617.4:c.508_516del MANE Select NP_002608.1:p.Gly170_Ala172del
NM_153818.2:c.508_516del NP_722540.1:p.Gly170_Ala172del
NR_164636.1:n.627_635del