Canonical Allele Identifier: CA1140725543

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406792T= , CM000663.2:g.2406792T=	GRCh38
NC_000001.10:g.2338231T= , CM000663.1:g.2338231T=	GRCh37
NC_000001.9:g.2328091T=	NCBI36
NG_008342.1:g.10780A=
NG_016128.1:g.20018T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.764A=	ENSP00000288774.3:p.Gln255=
ENST00000447513.7:c.704A= MANE Select	ENSP00000407922.2:p.Gln235=
ENST00000650293.1:c.658A=
ENST00000288774.7:c.764A=	ENSP00000288774.3:p.Gln255=
ENST00000447513.6:c.704A=	ENSP00000407922.2:p.Gln235=
ENST00000507596.5:c.704A=	ENSP00000424291.1:p.Gln235=
ENST00000510434.1:c.*70A=	ENSP00000423051.1:n.*70A=
NM_002617.3:c.704A=	NP_002608.1:p.Gln235=
NM_153818.1:c.764A=	NP_722540.1:p.Gln255=
XM_011541573.1:c.761A=	XP_011539875.1:p.Gln254=
XM_011541574.1:c.329A=	XP_011539876.1:p.Gln110=
XM_011541575.1:c.329A=	XP_011539877.1:p.Gln110=
XR_946666.1:n.820A=
XR_946666.2:n.769A=
NM_001374425.1:c.761A=	NP_001361354.1:p.Gln254=
NM_001374426.1:c.329A=	NP_001361355.1:p.Gln110=
NM_001374427.1:c.272A=	NP_001361356.1:p.Gln91=
NM_002617.4:c.704A= MANE Select	NP_002608.1:p.Gln235=
NM_153818.2:c.764A=	NP_722540.1:p.Gln255=
NR_164636.1:n.819A=