Canonical Allele Identifier: CA1140553047

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406553C= , CM000663.2:g.2406553C=	GRCh38
NC_000001.10:g.2337992C= , CM000663.1:g.2337992C=	GRCh37
NC_000001.9:g.2327852C=	NCBI36
NG_008342.1:g.11019G=
NG_016128.1:g.19779C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.903G=	ENSP00000288774.3:p.Arg301=
ENST00000447513.7:c.843G= MANE Select	ENSP00000407922.2:p.Arg281=
ENST00000650293.1:c.797G=
ENST00000288774.7:c.903G=	ENSP00000288774.3:p.Arg301=
ENST00000447513.6:c.843G=	ENSP00000407922.2:p.Arg281=
ENST00000507596.5:c.843G=	ENSP00000424291.1:p.Arg281=
ENST00000510434.1:c.*209G=	ENSP00000423051.1:n.*209G=
NM_002617.3:c.843G=	NP_002608.1:p.Arg281=
NM_153818.1:c.903G=	NP_722540.1:p.Arg301=
XM_011541573.1:c.900G=	XP_011539875.1:p.Arg300=
XM_011541574.1:c.468G=	XP_011539876.1:p.Arg156=
XM_011541575.1:c.468G=	XP_011539877.1:p.Arg156=
XR_946666.1:n.959G=
XR_946666.2:n.908G=
NM_001374425.1:c.900G=	NP_001361354.1:p.Arg300=
NM_001374426.1:c.468G=	NP_001361355.1:p.Arg156=
NM_001374427.1:c.411G=	NP_001361356.1:p.Arg137=
NM_002617.4:c.843G= MANE Select	NP_002608.1:p.Arg281=
NM_153818.2:c.903G=	NP_722540.1:p.Arg301=
NR_164636.1:n.958G=