Canonical Allele Identifier: CA1141101012

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406500G= , CM000663.2:g.2406500G=	GRCh38
NC_000001.10:g.2337939G= , CM000663.1:g.2337939G=	GRCh37
NC_000001.9:g.2327799G=	NCBI36
NG_008342.1:g.11072C=
NG_016128.1:g.19726G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.956C=	ENSP00000288774.3:p.Ala319=
ENST00000447513.7:c.896C= MANE Select	ENSP00000407922.2:p.Ala299=
ENST00000650293.1:c.850C=
ENST00000288774.7:c.956C=	ENSP00000288774.3:p.Ala319=
ENST00000447513.6:c.896C=	ENSP00000407922.2:p.Ala299=
ENST00000507596.5:c.896C=	ENSP00000424291.1:p.Ala299=
NM_002617.3:c.896C=	NP_002608.1:p.Ala299=
NM_153818.1:c.956C=	NP_722540.1:p.Ala319=
XM_011541573.1:c.953C=	XP_011539875.1:p.Ala318=
XM_011541574.1:c.521C=	XP_011539876.1:p.Ala174=
XM_011541575.1:c.521C=	XP_011539877.1:p.Ala174=
XR_946666.1:n.1012C=
XR_946666.2:n.961C=
NM_001374425.1:c.953C=	NP_001361354.1:p.Ala318=
NM_001374426.1:c.521C=	NP_001361355.1:p.Ala174=
NM_001374427.1:c.464C=	NP_001361356.1:p.Ala155=
NM_002617.4:c.896C= MANE Select	NP_002608.1:p.Ala299=
NM_153818.2:c.956C=	NP_722540.1:p.Ala319=
NR_164636.1:n.1011C=