Canonical Allele Identifier: CA1146736513

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408751C= , CM000663.2:g.2408751C=	GRCh38
NC_000001.10:g.2340190C= , CM000663.1:g.2340190C=	GRCh37
NC_000001.9:g.2330050C=	NCBI36
NG_008342.1:g.8821G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.301G=	ENSP00000288774.3:p.Val101=
ENST00000447513.7:c.301G= MANE Select	ENSP00000407922.2:p.Val101=
ENST00000650293.1:c.255G=
ENST00000288774.7:c.301G=	ENSP00000288774.3:p.Val101=
ENST00000447513.6:c.301G=	ENSP00000407922.2:p.Val101=
ENST00000502666.1:c.506G=	ENSP00000461951.1:n.506G=
ENST00000507596.5:c.301G=	ENSP00000424291.1:p.Val101=
ENST00000508384.5:c.-132G=	ENSP00000464289.1:n.-132G=
ENST00000510434.1:c.301G=	ENSP00000423051.1:p.Val101=
ENST00000515760.1:n.435G=
NM_002617.3:c.301G=	NP_002608.1:p.Val101=
NM_153818.1:c.301G=	NP_722540.1:p.Val101=
XM_011541573.1:c.301G=	XP_011539875.1:p.Val101=
XM_011541574.1:c.-132G=	XP_011539876.1:n.-132G=
XM_011541575.1:c.-132G=	XP_011539877.1:n.-132G=
XM_011541576.1:c.301G=	XP_011539878.1:p.Val101=
XR_946666.1:n.421G=
XM_011541576.2:c.301G=	XP_011539878.1:p.Val101=
XR_946666.2:n.370G=
NM_001374425.1:c.301G=	NP_001361354.1:p.Val101=
NM_001374426.1:c.-132G=	NP_001361355.1:n.-132G=
NM_001374427.1:c.-132G=	NP_001361356.1:n.-132G=
NM_002617.4:c.301G= MANE Select	NP_002608.1:p.Val101=
NM_153818.2:c.301G=	NP_722540.1:p.Val101=
NR_164636.1:n.420G=