Canonical Allele Identifier: CA1149570813

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406471G= , CM000663.2:g.2406471G=	GRCh38
NC_000001.10:g.2337910G= , CM000663.1:g.2337910G=	GRCh37
NC_000001.9:g.2327770G=	NCBI36
NG_008342.1:g.11101C=
NG_016128.1:g.19697G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.972+13C=	ENSP00000288774.3:n.972+13C=
ENST00000447513.7:c.912+13C= MANE Select	ENSP00000407922.2:n.912+13C=
ENST00000650293.1:c.866+13C=
ENST00000288774.7:c.972+13C=	ENSP00000288774.3:n.972+13C=
ENST00000447513.6:c.912+13C=	ENSP00000407922.2:n.912+13C=
ENST00000507596.5:c.912+13C=	ENSP00000424291.1:n.912+13C=
NM_002617.3:c.912+13C=	NP_002608.1:n.912+13C=
NM_153818.1:c.972+13C=	NP_722540.1:n.972+13C=
XM_011541573.1:c.969+13C=	XP_011539875.1:n.969+13C=
XM_011541574.1:c.537+13C=	XP_011539876.1:n.537+13C=
XM_011541575.1:c.537+13C=	XP_011539877.1:n.537+13C=
XR_946666.1:n.1028+13C=
XR_946666.2:n.977+13C=
NM_001374425.1:c.969+13C=	NP_001361354.1:n.969+13C=
NM_001374426.1:c.537+13C=	NP_001361355.1:n.537+13C=
NM_001374427.1:c.480+13C=	NP_001361356.1:n.480+13C=
NM_002617.4:c.912+13C= MANE Select	NP_002608.1:n.912+13C=
NM_153818.2:c.972+13C=	NP_722540.1:n.972+13C=
NR_164636.1:n.1027+13C=