Canonical Allele Identifier: CA1149570827

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406511C= , CM000663.2:g.2406511C=	GRCh38
NC_000001.10:g.2337950C= , CM000663.1:g.2337950C=	GRCh37
NC_000001.9:g.2327810C=	NCBI36
NG_008342.1:g.11061G=
NG_016128.1:g.19737C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.945G=	ENSP00000288774.3:p.Glu315=
ENST00000447513.7:c.885G= MANE Select	ENSP00000407922.2:p.Glu295=
ENST00000650293.1:c.839G=
ENST00000288774.7:c.945G=	ENSP00000288774.3:p.Glu315=
ENST00000447513.6:c.885G=	ENSP00000407922.2:p.Glu295=
ENST00000507596.5:c.885G=	ENSP00000424291.1:p.Glu295=
NM_002617.3:c.885G=	NP_002608.1:p.Glu295=
NM_153818.1:c.945G=	NP_722540.1:p.Glu315=
XM_011541573.1:c.942G=	XP_011539875.1:p.Glu314=
XM_011541574.1:c.510G=	XP_011539876.1:p.Glu170=
XM_011541575.1:c.510G=	XP_011539877.1:p.Glu170=
XR_946666.1:n.1001G=
XR_946666.2:n.950G=
NM_001374425.1:c.942G=	NP_001361354.1:p.Glu314=
NM_001374426.1:c.510G=	NP_001361355.1:p.Glu170=
NM_001374427.1:c.453G=	NP_001361356.1:p.Glu151=
NM_002617.4:c.885G= MANE Select	NP_002608.1:p.Glu295=
NM_153818.2:c.945G=	NP_722540.1:p.Glu315=
NR_164636.1:n.1000G=