Canonical Allele Identifier: CA1140504168

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406576T= , CM000663.2:g.2406576T=	GRCh38
NC_000001.10:g.2338015T= , CM000663.1:g.2338015T=	GRCh37
NC_000001.9:g.2327875T=	NCBI36
NG_008342.1:g.10996A=
NG_016128.1:g.19802T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.880A=	ENSP00000288774.3:p.Thr294=
ENST00000447513.7:c.820A= MANE Select	ENSP00000407922.2:p.Thr274=
ENST00000650293.1:c.774A=
ENST00000288774.7:c.880A=	ENSP00000288774.3:p.Thr294=
ENST00000447513.6:c.820A=	ENSP00000407922.2:p.Thr274=
ENST00000507596.5:c.820A=	ENSP00000424291.1:p.Thr274=
ENST00000510434.1:c.*186A=	ENSP00000423051.1:n.*186A=
NM_002617.3:c.820A=	NP_002608.1:p.Thr274=
NM_153818.1:c.880A=	NP_722540.1:p.Thr294=
XM_011541573.1:c.877A=	XP_011539875.1:p.Thr293=
XM_011541574.1:c.445A=	XP_011539876.1:p.Thr149=
XM_011541575.1:c.445A=	XP_011539877.1:p.Thr149=
XR_946666.1:n.936A=
XR_946666.2:n.885A=
NM_001374425.1:c.877A=	NP_001361354.1:p.Thr293=
NM_001374426.1:c.445A=	NP_001361355.1:p.Thr149=
NM_001374427.1:c.388A=	NP_001361356.1:p.Thr130=
NM_002617.4:c.820A= MANE Select	NP_002608.1:p.Thr274=
NM_153818.2:c.880A=	NP_722540.1:p.Thr294=
NR_164636.1:n.935A=