Canonical Allele Identifier: CA337984263

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406528G>A , CM000663.2:g.2406528G>A	GRCh38
NC_000001.10:g.2337967G>A , CM000663.1:g.2337967G>A	GRCh37
NC_000001.9:g.2327827G>A	NCBI36
NG_008342.1:g.11044C>T
NG_016128.1:g.19754G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.928C>T	ENSP00000288774.3:p.His310Tyr
ENST00000447513.7:c.868C>T MANE Select	ENSP00000407922.2:p.His290Tyr
ENST00000650293.1:c.822C>T
ENST00000288774.7:c.928C>T	ENSP00000288774.3:p.His310Tyr
ENST00000447513.6:c.868C>T	ENSP00000407922.2:p.His290Tyr
ENST00000507596.5:c.868C>T	ENSP00000424291.1:p.His290Tyr
ENST00000510434.1:c.*234C>T	ENSP00000423051.1:n.*234C>T
NM_002617.3:c.868C>T	NP_002608.1:p.His290Tyr
NM_153818.1:c.928C>T	NP_722540.1:p.His310Tyr
XM_011541573.1:c.925C>T	XP_011539875.1:p.His309Tyr
XM_011541574.1:c.493C>T	XP_011539876.1:p.His165Tyr
XM_011541575.1:c.493C>T	XP_011539877.1:p.His165Tyr
XR_946666.1:n.984C>T
XR_946666.2:n.933C>T
NM_001374425.1:c.925C>T	NP_001361354.1:p.His309Tyr
NM_001374426.1:c.493C>T	NP_001361355.1:p.His165Tyr
NM_001374427.1:c.436C>T	NP_001361356.1:p.His146Tyr
NM_002617.4:c.868C>T MANE Select	NP_002608.1:p.His290Tyr
NM_153818.2:c.928C>T	NP_722540.1:p.His310Tyr
NR_164636.1:n.983C>T