Canonical Allele Identifier: CA1149570808

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406464G= , CM000663.2:g.2406464G=	GRCh38
NC_000001.10:g.2337903G= , CM000663.1:g.2337903G=	GRCh37
NC_000001.9:g.2327763G=	NCBI36
NG_008342.1:g.11108C=
NG_016128.1:g.19690G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.972+20C=	ENSP00000288774.3:n.972+20C=
ENST00000447513.7:c.912+20C= MANE Select	ENSP00000407922.2:n.912+20C=
ENST00000650293.1:c.866+20C=
ENST00000288774.7:c.972+20C=	ENSP00000288774.3:n.972+20C=
ENST00000447513.6:c.912+20C=	ENSP00000407922.2:n.912+20C=
ENST00000507596.5:c.912+20C=	ENSP00000424291.1:n.912+20C=
NM_002617.3:c.912+20C=	NP_002608.1:n.912+20C=
NM_153818.1:c.972+20C=	NP_722540.1:n.972+20C=
XM_011541573.1:c.969+20C=	XP_011539875.1:n.969+20C=
XM_011541574.1:c.537+20C=	XP_011539876.1:n.537+20C=
XM_011541575.1:c.537+20C=	XP_011539877.1:n.537+20C=
XR_946666.1:n.1028+20C=
XR_946666.2:n.977+20C=
NM_001374425.1:c.969+20C=	NP_001361354.1:n.969+20C=
NM_001374426.1:c.537+20C=	NP_001361355.1:n.537+20C=
NM_001374427.1:c.480+20C=	NP_001361356.1:n.480+20C=
NM_002617.4:c.912+20C= MANE Select	NP_002608.1:n.912+20C=
NM_153818.2:c.972+20C=	NP_722540.1:n.972+20C=
NR_164636.1:n.1027+20C=