Canonical Allele Identifier: CA1141615313

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406502G= , CM000663.2:g.2406502G=	GRCh38
NC_000001.10:g.2337941G= , CM000663.1:g.2337941G=	GRCh37
NC_000001.9:g.2327801G=	NCBI36
NG_008342.1:g.11070C=
NG_016128.1:g.19728G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.954C=	ENSP00000288774.3:p.Thr318=
ENST00000447513.7:c.894C= MANE Select	ENSP00000407922.2:p.Thr298=
ENST00000650293.1:c.848C=
ENST00000288774.7:c.954C=	ENSP00000288774.3:p.Thr318=
ENST00000447513.6:c.894C=	ENSP00000407922.2:p.Thr298=
ENST00000507596.5:c.894C=	ENSP00000424291.1:p.Thr298=
NM_002617.3:c.894C=	NP_002608.1:p.Thr298=
NM_153818.1:c.954C=	NP_722540.1:p.Thr318=
XM_011541573.1:c.951C=	XP_011539875.1:p.Thr317=
XM_011541574.1:c.519C=	XP_011539876.1:p.Thr173=
XM_011541575.1:c.519C=	XP_011539877.1:p.Thr173=
XR_946666.1:n.1010C=
XR_946666.2:n.959C=
NM_001374425.1:c.951C=	NP_001361354.1:p.Thr317=
NM_001374426.1:c.519C=	NP_001361355.1:p.Thr173=
NM_001374427.1:c.462C=	NP_001361356.1:p.Thr154=
NM_002617.4:c.894C= MANE Select	NP_002608.1:p.Thr298=
NM_153818.2:c.954C=	NP_722540.1:p.Thr318=
NR_164636.1:n.1009C=