Canonical Allele Identifier: CA1149571835

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408588T= , CM000663.2:g.2408588T=	GRCh38
NC_000001.10:g.2340027T= , CM000663.1:g.2340027T=	GRCh37
NC_000001.9:g.2329887T=	NCBI36
NG_008342.1:g.8984A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.464A=	ENSP00000288774.3:p.Gln155=
ENST00000447513.7:c.464A= MANE Select	ENSP00000407922.2:p.Gln155=
ENST00000650293.1:c.418A=
ENST00000288774.7:c.464A=	ENSP00000288774.3:p.Gln155=
ENST00000447513.6:c.464A=	ENSP00000407922.2:p.Gln155=
ENST00000507596.5:c.464A=	ENSP00000424291.1:p.Gln155=
ENST00000508384.5:c.32A=	ENSP00000464289.1:p.Gln11=
ENST00000510434.1:c.464A=	ENSP00000423051.1:p.Gln155=
ENST00000515760.1:n.598A=
NM_002617.3:c.464A=	NP_002608.1:p.Gln155=
NM_153818.1:c.464A=	NP_722540.1:p.Gln155=
XM_011541573.1:c.464A=	XP_011539875.1:p.Gln155=
XM_011541574.1:c.32A=	XP_011539876.1:p.Gln11=
XM_011541575.1:c.32A=	XP_011539877.1:p.Gln11=
XM_011541576.1:c.464A=	XP_011539878.1:p.Gln155=
XR_946666.1:n.584A=
XM_011541576.2:c.464A=	XP_011539878.1:p.Gln155=
XR_946666.2:n.533A=
NM_001374425.1:c.464A=	NP_001361354.1:p.Gln155=
NM_001374426.1:c.32A=	NP_001361355.1:p.Gln11=
NM_001374427.1:c.32A=	NP_001361356.1:p.Gln11=
NM_002617.4:c.464A= MANE Select	NP_002608.1:p.Gln155=
NM_153818.2:c.464A=	NP_722540.1:p.Gln155=
NR_164636.1:n.583A=