Canonical Allele Identifier: CA1140725539

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406528G= , CM000663.2:g.2406528G=	GRCh38
NC_000001.10:g.2337967G= , CM000663.1:g.2337967G=	GRCh37
NC_000001.9:g.2327827G=	NCBI36
NG_008342.1:g.11044C=
NG_016128.1:g.19754G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.928C=	ENSP00000288774.3:p.His310=
ENST00000447513.7:c.868C= MANE Select	ENSP00000407922.2:p.His290=
ENST00000650293.1:c.822C=
ENST00000288774.7:c.928C=	ENSP00000288774.3:p.His310=
ENST00000447513.6:c.868C=	ENSP00000407922.2:p.His290=
ENST00000507596.5:c.868C=	ENSP00000424291.1:p.His290=
ENST00000510434.1:c.*234C=	ENSP00000423051.1:n.*234C=
NM_002617.3:c.868C=	NP_002608.1:p.His290=
NM_153818.1:c.928C=	NP_722540.1:p.His310=
XM_011541573.1:c.925C=	XP_011539875.1:p.His309=
XM_011541574.1:c.493C=	XP_011539876.1:p.His165=
XM_011541575.1:c.493C=	XP_011539877.1:p.His165=
XR_946666.1:n.984C=
XR_946666.2:n.933C=
NM_001374425.1:c.925C=	NP_001361354.1:p.His309=
NM_001374426.1:c.493C=	NP_001361355.1:p.His165=
NM_001374427.1:c.436C=	NP_001361356.1:p.His146=
NM_002617.4:c.868C= MANE Select	NP_002608.1:p.His290=
NM_153818.2:c.928C=	NP_722540.1:p.His310=
NR_164636.1:n.983C=