Canonical Allele Identifier: CA1149571917

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408791G= , CM000663.2:g.2408791G=	GRCh38
NC_000001.10:g.2340230G= , CM000663.1:g.2340230G=	GRCh37
NC_000001.9:g.2330090G=	NCBI36
NG_008342.1:g.8781C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.261C=	ENSP00000288774.3:p.Pro87=
ENST00000447513.7:c.261C= MANE Select	ENSP00000407922.2:p.Pro87=
ENST00000650293.1:c.215C=
ENST00000288774.7:c.261C=	ENSP00000288774.3:p.Pro87=
ENST00000447513.6:c.261C=	ENSP00000407922.2:p.Pro87=
ENST00000502666.1:c.466C=	ENSP00000461951.1:n.466C=
ENST00000507596.5:c.261C=	ENSP00000424291.1:p.Pro87=
ENST00000508384.5:c.-172C=	ENSP00000464289.1:n.-172C=
ENST00000510434.1:c.261C=	ENSP00000423051.1:p.Pro87=
ENST00000514502.1:c.*278C=	ENSP00000425924.1:n.*278C=
ENST00000515760.1:n.395C=
NM_002617.3:c.261C=	NP_002608.1:p.Pro87=
NM_153818.1:c.261C=	NP_722540.1:p.Pro87=
XM_011541573.1:c.261C=	XP_011539875.1:p.Pro87=
XM_011541574.1:c.-172C=	XP_011539876.1:n.-172C=
XM_011541575.1:c.-172C=	XP_011539877.1:n.-172C=
XM_011541576.1:c.261C=	XP_011539878.1:p.Pro87=
XR_946666.1:n.381C=
XM_011541576.2:c.261C=	XP_011539878.1:p.Pro87=
XR_946666.2:n.330C=
NM_001374425.1:c.261C=	NP_001361354.1:p.Pro87=
NM_001374426.1:c.-172C=	NP_001361355.1:n.-172C=
NM_001374427.1:c.-172C=	NP_001361356.1:n.-172C=
NM_002617.4:c.261C= MANE Select	NP_002608.1:p.Pro87=
NM_153818.2:c.261C=	NP_722540.1:p.Pro87=
NR_164636.1:n.380C=