Canonical Allele Identifier: CA1140725542

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406766G= , CM000663.2:g.2406766G=	GRCh38
NC_000001.10:g.2338205G= , CM000663.1:g.2338205G=	GRCh37
NC_000001.9:g.2328065G=	NCBI36
NG_008342.1:g.10806C=
NG_016128.1:g.19992G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.790C=	ENSP00000288774.3:p.Arg264=
ENST00000447513.7:c.730C= MANE Select	ENSP00000407922.2:p.Arg244=
ENST00000650293.1:c.684C=
ENST00000288774.7:c.790C=	ENSP00000288774.3:p.Arg264=
ENST00000447513.6:c.730C=	ENSP00000407922.2:p.Arg244=
ENST00000507596.5:c.730C=	ENSP00000424291.1:p.Arg244=
ENST00000510434.1:c.*96C=	ENSP00000423051.1:n.*96C=
NM_002617.3:c.730C=	NP_002608.1:p.Arg244=
NM_153818.1:c.790C=	NP_722540.1:p.Arg264=
XM_011541573.1:c.787C=	XP_011539875.1:p.Arg263=
XM_011541574.1:c.355C=	XP_011539876.1:p.Arg119=
XM_011541575.1:c.355C=	XP_011539877.1:p.Arg119=
XR_946666.1:n.846C=
XR_946666.2:n.795C=
NM_001374425.1:c.787C=	NP_001361354.1:p.Arg263=
NM_001374426.1:c.355C=	NP_001361355.1:p.Arg119=
NM_001374427.1:c.298C=	NP_001361356.1:p.Arg100=
NM_002617.4:c.730C= MANE Select	NP_002608.1:p.Arg244=
NM_153818.2:c.790C=	NP_722540.1:p.Arg264=
NR_164636.1:n.845C=