Canonical Allele Identifier: CA1146832314

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406624G= , CM000663.2:g.2406624G=	GRCh38
NC_000001.10:g.2338063G= , CM000663.1:g.2338063G=	GRCh37
NC_000001.9:g.2327923G=	NCBI36
NG_008342.1:g.10948C=
NG_016128.1:g.19850G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.837-5C=	ENSP00000288774.3:n.837-5C=
ENST00000447513.7:c.777-5C= MANE Select	ENSP00000407922.2:n.777-5C=
ENST00000650293.1:c.731-5C=
ENST00000288774.7:c.837-5C=	ENSP00000288774.3:n.837-5C=
ENST00000447513.6:c.777-5C=	ENSP00000407922.2:n.777-5C=
ENST00000507596.5:c.777-5C=	ENSP00000424291.1:n.777-5C=
ENST00000510434.1:c.*143-5C=	ENSP00000423051.1:n.*143-5C=
NM_002617.3:c.777-5C=	NP_002608.1:n.777-5C=
NM_153818.1:c.837-5C=	NP_722540.1:n.837-5C=
XM_011541573.1:c.834-5C=	XP_011539875.1:n.834-5C=
XM_011541574.1:c.402-5C=	XP_011539876.1:n.402-5C=
XM_011541575.1:c.402-5C=	XP_011539877.1:n.402-5C=
XR_946666.1:n.893-5C=
XR_946666.2:n.842-5C=
NM_001374425.1:c.834-5C=	NP_001361354.1:n.834-5C=
NM_001374426.1:c.402-5C=	NP_001361355.1:n.402-5C=
NM_001374427.1:c.345-5C=	NP_001361356.1:n.345-5C=
NM_002617.4:c.777-5C= MANE Select	NP_002608.1:n.777-5C=
NM_153818.2:c.837-5C=	NP_722540.1:n.837-5C=
NR_164636.1:n.892-5C=