Canonical Allele Identifier: CA1149571881

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408698_2408700delinsCTG , CM000663.2:g.2408698_2408700delinsCTG	GRCh38
NC_000001.10:g.2340137_2340139delinsCTG , CM000663.1:g.2340137_2340139delinsCTG	GRCh37
NC_000001.9:g.2329997_2329999delinsCTG	NCBI36
NG_008342.1:g.8872_8874delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.352_354delinsCAG	ENSP00000288774.3:p.Gln118=
ENST00000447513.7:c.352_354delinsCAG MANE Select	ENSP00000407922.2:p.Gln118=
ENST00000650293.1:c.306_308delinsCAG
ENST00000288774.7:c.352_354delinsCAG	ENSP00000288774.3:p.Gln118=
ENST00000447513.6:c.352_354delinsCAG	ENSP00000407922.2:p.Gln118=
ENST00000502666.1:c.557_559delinsCAG	ENSP00000461951.1:n.557_559delinsCAG
ENST00000507596.5:c.352_354delinsCAG	ENSP00000424291.1:p.Gln118=
ENST00000508384.5:c.-81_-79delinsCAG	ENSP00000464289.1:n.-81_-79delinsCAG
ENST00000510434.1:c.352_354delinsCAG	ENSP00000423051.1:p.Gln118=
ENST00000515760.1:n.486_488delinsCAG
NM_002617.3:c.352_354delinsCAG	NP_002608.1:p.Gln118=
NM_153818.1:c.352_354delinsCAG	NP_722540.1:p.Gln118=
XM_011541573.1:c.352_354delinsCAG	XP_011539875.1:p.Gln118=
XM_011541574.1:c.-81_-79delinsCAG	XP_011539876.1:n.-81_-79delinsCAG
XM_011541575.1:c.-81_-79delinsCAG	XP_011539877.1:n.-81_-79delinsCAG
XM_011541576.1:c.352_354delinsCAG	XP_011539878.1:p.Gln118=
XR_946666.1:n.472_474delinsCAG
XM_011541576.2:c.352_354delinsCAG	XP_011539878.1:p.Gln118=
XR_946666.2:n.421_423delinsCAG
NM_001374425.1:c.352_354delinsCAG	NP_001361354.1:p.Gln118=
NM_001374426.1:c.-81_-79delinsCAG	NP_001361355.1:n.-81_-79delinsCAG
NM_001374427.1:c.-81_-79delinsCAG	NP_001361356.1:n.-81_-79delinsCAG
NM_002617.4:c.352_354delinsCAG MANE Select	NP_002608.1:p.Gln118=
NM_153818.2:c.352_354delinsCAG	NP_722540.1:p.Gln118=
NR_164636.1:n.471_473delinsCAG