Canonical Allele Identifier: CA1149571708

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408339G= , CM000663.2:g.2408339G=	GRCh38
NC_000001.10:g.2339778G= , CM000663.1:g.2339778G=	GRCh37
NC_000001.9:g.2329638G=	NCBI36
NG_008342.1:g.9233C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.600+113C=	ENSP00000288774.3:n.600+113C=
ENST00000447513.7:c.600+113C= MANE Select	ENSP00000407922.2:n.600+113C=
ENST00000650293.1:c.554+113C=
ENST00000288774.7:c.600+113C=	ENSP00000288774.3:n.600+113C=
ENST00000447513.6:c.600+113C=	ENSP00000407922.2:n.600+113C=
ENST00000507596.5:c.600+113C=	ENSP00000424291.1:n.600+113C=
ENST00000510434.1:c.596+117C=	ENSP00000423051.1:n.596+117C=
NM_002617.3:c.600+113C=	NP_002608.1:n.600+113C=
NM_153818.1:c.600+113C=	NP_722540.1:n.600+113C=
XM_011541573.1:c.600+113C=	XP_011539875.1:n.600+113C=
XM_011541574.1:c.168+113C=	XP_011539876.1:n.168+113C=
XM_011541575.1:c.168+113C=	XP_011539877.1:n.168+113C=
XM_011541576.1:c.596+117C=	XP_011539878.1:n.596+117C=
XR_946666.1:n.716+117C=
XM_011541576.2:c.596+117C=	XP_011539878.1:n.596+117C=
XR_946666.2:n.665+117C=
NM_001374425.1:c.600+113C=	NP_001361354.1:n.600+113C=
NM_001374426.1:c.168+113C=	NP_001361355.1:n.168+113C=
NM_001374427.1:c.168+113C=	NP_001361356.1:n.168+113C=
NM_002617.4:c.600+113C= MANE Select	NP_002608.1:n.600+113C=
NM_153818.2:c.600+113C=	NP_722540.1:n.600+113C=
NR_164636.1:n.715+117C=