Canonical Allele Identifier: CA337984744

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406606C>A , CM000663.2:g.2406606C>A	GRCh38
NC_000001.10:g.2338045C>A , CM000663.1:g.2338045C>A	GRCh37
NC_000001.9:g.2327905C>A	NCBI36
NG_008342.1:g.10966G>T
NG_016128.1:g.19832C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002617.4:c.790G>T MANE Select	NP_002608.1:p.Glu264Ter
ENST00000447513.7:c.790G>T MANE Select	ENSP00000407922.2:p.Glu264Ter
NM_001374425.1:c.847G>T	NP_001361354.1:p.Glu283Ter
NM_001374426.1:c.415G>T	NP_001361355.1:p.Glu139Ter
NM_001374427.1:c.358G>T	NP_001361356.1:p.Glu120Ter
NM_002617.3:c.790G>T	NP_002608.1:p.Glu264Ter
NM_153818.1:c.850G>T	NP_722540.1:p.Glu284Ter
NM_153818.2:c.850G>T	NP_722540.1:p.Glu284Ter
NR_164636.1:n.905G>T
ENST00000288774.7:c.850G>T	ENSP00000288774.3:p.Glu284Ter
ENST00000288774.8:c.850G>T	ENSP00000288774.3:p.Glu284Ter
ENST00000447513.6:c.790G>T	ENSP00000407922.2:p.Glu264Ter
ENST00000507596.5:c.790G>T	ENSP00000424291.1:p.Glu264Ter
ENST00000510434.1:c.*156G>T	ENSP00000423051.1:n.*156G>T
ENST00000650293.1:c.744G>T
XM_011541573.1:c.847G>T	XP_011539875.1:p.Glu283Ter
XM_011541574.1:c.415G>T	XP_011539876.1:p.Glu139Ter
XM_011541575.1:c.415G>T	XP_011539877.1:p.Glu139Ter
XR_946666.1:n.906G>T
XR_946666.2:n.855G>T