Canonical Allele Identifier: CA1140762424

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406561C= , CM000663.2:g.2406561C=	GRCh38
NC_000001.10:g.2338000C= , CM000663.1:g.2338000C=	GRCh37
NC_000001.9:g.2327860C=	NCBI36
NG_008342.1:g.11011G=
NG_016128.1:g.19787C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.895G=	ENSP00000288774.3:p.Glu299=
ENST00000447513.7:c.835G= MANE Select	ENSP00000407922.2:p.Glu279=
ENST00000650293.1:c.789G=
ENST00000288774.7:c.895G=	ENSP00000288774.3:p.Glu299=
ENST00000447513.6:c.835G=	ENSP00000407922.2:p.Glu279=
ENST00000507596.5:c.835G=	ENSP00000424291.1:p.Glu279=
ENST00000510434.1:c.*201G=	ENSP00000423051.1:n.*201G=
NM_002617.3:c.835G=	NP_002608.1:p.Glu279=
NM_153818.1:c.895G=	NP_722540.1:p.Glu299=
XM_011541573.1:c.892G=	XP_011539875.1:p.Glu298=
XM_011541574.1:c.460G=	XP_011539876.1:p.Glu154=
XM_011541575.1:c.460G=	XP_011539877.1:p.Glu154=
XR_946666.1:n.951G=
XR_946666.2:n.900G=
NM_001374425.1:c.892G=	NP_001361354.1:p.Glu298=
NM_001374426.1:c.460G=	NP_001361355.1:p.Glu154=
NM_001374427.1:c.403G=	NP_001361356.1:p.Glu135=
NM_002617.4:c.835G= MANE Select	NP_002608.1:p.Glu279=
NM_153818.2:c.895G=	NP_722540.1:p.Glu299=
NR_164636.1:n.950G=