Canonical Allele Identifier: CA1149570820

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406492T= , CM000663.2:g.2406492T=	GRCh38
NC_000001.10:g.2337931T= , CM000663.1:g.2337931T=	GRCh37
NC_000001.9:g.2327791T=	NCBI36
NG_008342.1:g.11080A=
NG_016128.1:g.19718T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.964A=	ENSP00000288774.3:p.Ser322=
ENST00000447513.7:c.904A= MANE Select	ENSP00000407922.2:p.Ser302=
ENST00000650293.1:c.858A=
ENST00000288774.7:c.964A=	ENSP00000288774.3:p.Ser322=
ENST00000447513.6:c.904A=	ENSP00000407922.2:p.Ser302=
ENST00000507596.5:c.904A=	ENSP00000424291.1:p.Ser302=
NM_002617.3:c.904A=	NP_002608.1:p.Ser302=
NM_153818.1:c.964A=	NP_722540.1:p.Ser322=
XM_011541573.1:c.961A=	XP_011539875.1:p.Ser321=
XM_011541574.1:c.529A=	XP_011539876.1:p.Ser177=
XM_011541575.1:c.529A=	XP_011539877.1:p.Ser177=
XR_946666.1:n.1020A=
XR_946666.2:n.969A=
NM_001374425.1:c.961A=	NP_001361354.1:p.Ser321=
NM_001374426.1:c.529A=	NP_001361355.1:p.Ser177=
NM_001374427.1:c.472A=	NP_001361356.1:p.Ser158=
NM_002617.4:c.904A= MANE Select	NP_002608.1:p.Ser302=
NM_153818.2:c.964A=	NP_722540.1:p.Ser322=
NR_164636.1:n.1019A=