Canonical Allele Identifier: CA1149571929

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408828C= , CM000663.2:g.2408828C=	GRCh38
NC_000001.10:g.2340267C= , CM000663.1:g.2340267C=	GRCh37
NC_000001.9:g.2330127C=	NCBI36
NG_008342.1:g.8744G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.224G=	ENSP00000288774.3:p.Ser75=
ENST00000447513.7:c.224G= MANE Select	ENSP00000407922.2:p.Ser75=
ENST00000650293.1:c.178G=
ENST00000288774.7:c.224G=	ENSP00000288774.3:p.Ser75=
ENST00000447513.6:c.224G=	ENSP00000407922.2:p.Ser75=
ENST00000502666.1:c.429G=	ENSP00000461951.1:n.429G=
ENST00000507596.5:c.224G=	ENSP00000424291.1:p.Ser75=
ENST00000508384.5:c.-209G=	ENSP00000464289.1:n.-209G=
ENST00000510434.1:c.224G=	ENSP00000423051.1:p.Ser75=
ENST00000514502.1:c.*241G=	ENSP00000425924.1:n.*241G=
ENST00000515760.1:n.358G=
NM_002617.3:c.224G=	NP_002608.1:p.Ser75=
NM_153818.1:c.224G=	NP_722540.1:p.Ser75=
XM_011541573.1:c.224G=	XP_011539875.1:p.Ser75=
XM_011541574.1:c.-209G=	XP_011539876.1:n.-209G=
XM_011541575.1:c.-209G=	XP_011539877.1:n.-209G=
XM_011541576.1:c.224G=	XP_011539878.1:p.Ser75=
XR_946666.1:n.344G=
XM_011541576.2:c.224G=	XP_011539878.1:p.Ser75=
XR_946666.2:n.293G=
NM_001374425.1:c.224G=	NP_001361354.1:p.Ser75=
NM_001374426.1:c.-209G=	NP_001361355.1:n.-209G=
NM_001374427.1:c.-209G=	NP_001361356.1:n.-209G=
NM_002617.4:c.224G= MANE Select	NP_002608.1:p.Ser75=
NM_153818.2:c.224G=	NP_722540.1:p.Ser75=
NR_164636.1:n.343G=