Canonical Allele Identifier: CA1149570825

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406508G= , CM000663.2:g.2406508G=	GRCh38
NC_000001.10:g.2337947G= , CM000663.1:g.2337947G=	GRCh37
NC_000001.9:g.2327807G=	NCBI36
NG_008342.1:g.11064C=
NG_016128.1:g.19734G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.948C=	ENSP00000288774.3:p.Cys316=
ENST00000447513.7:c.888C= MANE Select	ENSP00000407922.2:p.Cys296=
ENST00000650293.1:c.842C=
ENST00000288774.7:c.948C=	ENSP00000288774.3:p.Cys316=
ENST00000447513.6:c.888C=	ENSP00000407922.2:p.Cys296=
ENST00000507596.5:c.888C=	ENSP00000424291.1:p.Cys296=
NM_002617.3:c.888C=	NP_002608.1:p.Cys296=
NM_153818.1:c.948C=	NP_722540.1:p.Cys316=
XM_011541573.1:c.945C=	XP_011539875.1:p.Cys315=
XM_011541574.1:c.513C=	XP_011539876.1:p.Cys171=
XM_011541575.1:c.513C=	XP_011539877.1:p.Cys171=
XR_946666.1:n.1004C=
XR_946666.2:n.953C=
NM_001374425.1:c.945C=	NP_001361354.1:p.Cys315=
NM_001374426.1:c.513C=	NP_001361355.1:p.Cys171=
NM_001374427.1:c.456C=	NP_001361356.1:p.Cys152=
NM_002617.4:c.888C= MANE Select	NP_002608.1:p.Cys296=
NM_153818.2:c.948C=	NP_722540.1:p.Cys316=
NR_164636.1:n.1003C=