Canonical Allele Identifier: CA1149571771

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408455C= , CM000663.2:g.2408455C=	GRCh38
NC_000001.10:g.2339894C= , CM000663.1:g.2339894C=	GRCh37
NC_000001.9:g.2329754C=	NCBI36
NG_008342.1:g.9117G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.597G=	ENSP00000288774.3:p.Thr199=
ENST00000447513.7:c.597G= MANE Select	ENSP00000407922.2:p.Thr199=
ENST00000650293.1:c.551G=
ENST00000288774.7:c.597G=	ENSP00000288774.3:p.Thr199=
ENST00000447513.6:c.597G=	ENSP00000407922.2:p.Thr199=
ENST00000507596.5:c.597G=	ENSP00000424291.1:p.Thr199=
ENST00000510434.1:c.596+1G=	ENSP00000423051.1:n.596+1G=
NM_002617.3:c.597G=	NP_002608.1:p.Thr199=
NM_153818.1:c.597G=	NP_722540.1:p.Thr199=
XM_011541573.1:c.597G=	XP_011539875.1:p.Thr199=
XM_011541574.1:c.165G=	XP_011539876.1:p.Thr55=
XM_011541575.1:c.165G=	XP_011539877.1:p.Thr55=
XM_011541576.1:c.596+1G=	XP_011539878.1:n.596+1G=
XR_946666.1:n.716+1G=
XM_011541576.2:c.596+1G=	XP_011539878.1:n.596+1G=
XR_946666.2:n.665+1G=
NM_001374425.1:c.597G=	NP_001361354.1:p.Thr199=
NM_001374426.1:c.165G=	NP_001361355.1:p.Thr55=
NM_001374427.1:c.165G=	NP_001361356.1:p.Thr55=
NM_002617.4:c.597G= MANE Select	NP_002608.1:p.Thr199=
NM_153818.2:c.597G=	NP_722540.1:p.Thr199=
NR_164636.1:n.715+1G=