Canonical Allele Identifier: CA1149571845

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408608_2408620delinsGTGGTGACGCATC , CM000663.2:g.2408608_2408620delinsGTGGTGACGCATC	GRCh38
NC_000001.10:g.2340047_2340059delinsGTGGTGACGCATC , CM000663.1:g.2340047_2340059delinsGTGGTGACGCATC	GRCh37
NC_000001.9:g.2329907_2329919delinsGTGGTGACGCATC	NCBI36
NG_008342.1:g.8952_8964delinsGATGCGTCACCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.432_444delinsGATGCGTCACCAC	ENSP00000288774.3:p.Trp144=
ENST00000447513.7:c.432_444delinsGATGCGTCACCAC MANE Select	ENSP00000407922.2:p.Trp144=
ENST00000650293.1:c.386_398delinsGATGCGTCACCAC
ENST00000288774.7:c.432_444delinsGATGCGTCACCAC	ENSP00000288774.3:p.Trp144=
ENST00000447513.6:c.432_444delinsGATGCGTCACCAC	ENSP00000407922.2:p.Trp144=
ENST00000502666.1:c.637_649delinsGATGCGTCACCAC	ENSP00000461951.1:n.637_649delinsGATGCGTCACCAC
ENST00000507596.5:c.432_444delinsGATGCGTCACCAC	ENSP00000424291.1:p.Trp144=
ENST00000508384.5:c.-1_12delinsGATGCGTCACCAC
ENST00000510434.1:c.432_444delinsGATGCGTCACCAC	ENSP00000423051.1:p.Trp144=
ENST00000515760.1:n.566_578delinsGATGCGTCACCAC
NM_002617.3:c.432_444delinsGATGCGTCACCAC	NP_002608.1:p.Trp144=
NM_153818.1:c.432_444delinsGATGCGTCACCAC	NP_722540.1:p.Trp144=
XM_011541573.1:c.432_444delinsGATGCGTCACCAC	XP_011539875.1:p.Trp144=
XM_011541574.1:c.-1_12delinsGATGCGTCACCAC
XM_011541575.1:c.-1_12delinsGATGCGTCACCAC
XM_011541576.1:c.432_444delinsGATGCGTCACCAC	XP_011539878.1:p.Trp144=
XR_946666.1:n.552_564delinsGATGCGTCACCAC
XM_011541576.2:c.432_444delinsGATGCGTCACCAC	XP_011539878.1:p.Trp144=
XR_946666.2:n.501_513delinsGATGCGTCACCAC
NM_001374425.1:c.432_444delinsGATGCGTCACCAC	NP_001361354.1:p.Trp144=
NM_001374426.1:c.-1_12delinsGATGCGTCACCAC
NM_001374427.1:c.-1_12delinsGATGCGTCACCAC
NM_002617.4:c.432_444delinsGATGCGTCACCAC MANE Select	NP_002608.1:p.Trp144=
NM_153818.2:c.432_444delinsGATGCGTCACCAC	NP_722540.1:p.Trp144=
NR_164636.1:n.551_563delinsGATGCGTCACCAC