Canonical Allele Identifier: CA1148224148

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2405815C= , CM000663.2:g.2405815C=	GRCh38
NC_000001.10:g.2337254C= , CM000663.1:g.2337254C=	GRCh37
NC_000001.9:g.2327114C=	NCBI36
NG_008342.1:g.11757G=
NG_016128.1:g.19041C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.992G=	ENSP00000288774.3:p.Arg331=
ENST00000447513.7:c.932G= MANE Select	ENSP00000407922.2:p.Arg311=
ENST00000650293.1:c.886G=
ENST00000288774.7:c.992G=	ENSP00000288774.3:p.Arg331=
ENST00000447513.6:c.932G=	ENSP00000407922.2:p.Arg311=
ENST00000507596.5:c.926G=	ENSP00000424291.1:p.Arg309=
NM_002617.3:c.932G=	NP_002608.1:p.Arg311=
NM_153818.1:c.992G=	NP_722540.1:p.Arg331=
XM_011541573.1:c.989G=	XP_011539875.1:p.Arg330=
XM_011541574.1:c.557G=	XP_011539876.1:p.Arg186=
XM_011541575.1:c.557G=	XP_011539877.1:p.Arg186=
XR_946666.1:n.1048G=
XR_946666.2:n.997G=
NM_001374425.1:c.989G=	NP_001361354.1:p.Arg330=
NM_001374426.1:c.557G=	NP_001361355.1:p.Arg186=
NM_001374427.1:c.500G=	NP_001361356.1:p.Arg167=
NM_002617.4:c.932G= MANE Select	NP_002608.1:p.Arg311=
NM_153818.2:c.992G=	NP_722540.1:p.Arg331=
NR_164636.1:n.1047G=