Canonical Allele Identifier: CA1149570830

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406523C= , CM000663.2:g.2406523C=	GRCh38
NC_000001.10:g.2337962C= , CM000663.1:g.2337962C=	GRCh37
NC_000001.9:g.2327822C=	NCBI36
NG_008342.1:g.11049G=
NG_016128.1:g.19749C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.933G=	ENSP00000288774.3:p.Leu311=
ENST00000447513.7:c.873G= MANE Select	ENSP00000407922.2:p.Leu291=
ENST00000650293.1:c.827G=
ENST00000288774.7:c.933G=	ENSP00000288774.3:p.Leu311=
ENST00000447513.6:c.873G=	ENSP00000407922.2:p.Leu291=
ENST00000507596.5:c.873G=	ENSP00000424291.1:p.Leu291=
ENST00000510434.1:c.*239G=	ENSP00000423051.1:n.*239G=
NM_002617.3:c.873G=	NP_002608.1:p.Leu291=
NM_153818.1:c.933G=	NP_722540.1:p.Leu311=
XM_011541573.1:c.930G=	XP_011539875.1:p.Leu310=
XM_011541574.1:c.498G=	XP_011539876.1:p.Leu166=
XM_011541575.1:c.498G=	XP_011539877.1:p.Leu166=
XR_946666.1:n.989G=
XR_946666.2:n.938G=
NM_001374425.1:c.930G=	NP_001361354.1:p.Leu310=
NM_001374426.1:c.498G=	NP_001361355.1:p.Leu166=
NM_001374427.1:c.441G=	NP_001361356.1:p.Leu147=
NM_002617.4:c.873G= MANE Select	NP_002608.1:p.Leu291=
NM_153818.2:c.933G=	NP_722540.1:p.Leu311=
NR_164636.1:n.988G=