Canonical Allele Identifier: CA1148224149

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406566A= , CM000663.2:g.2406566A=	GRCh38
NC_000001.10:g.2338005A= , CM000663.1:g.2338005A=	GRCh37
NC_000001.9:g.2327865A=	NCBI36
NG_008342.1:g.11006T=
NG_016128.1:g.19792A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.890T=	ENSP00000288774.3:p.Leu297=
ENST00000447513.7:c.830T= MANE Select	ENSP00000407922.2:p.Leu277=
ENST00000650293.1:c.784T=
ENST00000288774.7:c.890T=	ENSP00000288774.3:p.Leu297=
ENST00000447513.6:c.830T=	ENSP00000407922.2:p.Leu277=
ENST00000507596.5:c.830T=	ENSP00000424291.1:p.Leu277=
ENST00000510434.1:c.*196T=	ENSP00000423051.1:n.*196T=
NM_002617.3:c.830T=	NP_002608.1:p.Leu277=
NM_153818.1:c.890T=	NP_722540.1:p.Leu297=
XM_011541573.1:c.887T=	XP_011539875.1:p.Leu296=
XM_011541574.1:c.455T=	XP_011539876.1:p.Leu152=
XM_011541575.1:c.455T=	XP_011539877.1:p.Leu152=
XR_946666.1:n.946T=
XR_946666.2:n.895T=
NM_001374425.1:c.887T=	NP_001361354.1:p.Leu296=
NM_001374426.1:c.455T=	NP_001361355.1:p.Leu152=
NM_001374427.1:c.398T=	NP_001361356.1:p.Leu133=
NM_002617.4:c.830T= MANE Select	NP_002608.1:p.Leu277=
NM_153818.2:c.890T=	NP_722540.1:p.Leu297=
NR_164636.1:n.945T=