Canonical Allele Identifier: CA1140725536

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406515C= , CM000663.2:g.2406515C=	GRCh38
NC_000001.10:g.2337954C= , CM000663.1:g.2337954C=	GRCh37
NC_000001.9:g.2327814C=	NCBI36
NG_008342.1:g.11057G=
NG_016128.1:g.19741C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.941G=	ENSP00000288774.3:p.Trp314=
ENST00000447513.7:c.881G= MANE Select	ENSP00000407922.2:p.Trp294=
ENST00000650293.1:c.835G=
ENST00000288774.7:c.941G=	ENSP00000288774.3:p.Trp314=
ENST00000447513.6:c.881G=	ENSP00000407922.2:p.Trp294=
ENST00000507596.5:c.881G=	ENSP00000424291.1:p.Trp294=
NM_002617.3:c.881G=	NP_002608.1:p.Trp294=
NM_153818.1:c.941G=	NP_722540.1:p.Trp314=
XM_011541573.1:c.938G=	XP_011539875.1:p.Trp313=
XM_011541574.1:c.506G=	XP_011539876.1:p.Trp169=
XM_011541575.1:c.506G=	XP_011539877.1:p.Trp169=
XR_946666.1:n.997G=
XR_946666.2:n.946G=
NM_001374425.1:c.938G=	NP_001361354.1:p.Trp313=
NM_001374426.1:c.506G=	NP_001361355.1:p.Trp169=
NM_001374427.1:c.449G=	NP_001361356.1:p.Trp150=
NM_002617.4:c.881G= MANE Select	NP_002608.1:p.Trp294=
NM_153818.2:c.941G=	NP_722540.1:p.Trp314=
NR_164636.1:n.996G=