Canonical Allele Identifier: CA1149570837

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406541G= , CM000663.2:g.2406541G=	GRCh38
NC_000001.10:g.2337980G= , CM000663.1:g.2337980G=	GRCh37
NC_000001.9:g.2327840G=	NCBI36
NG_008342.1:g.11031C=
NG_016128.1:g.19767G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.915C=	ENSP00000288774.3:p.Ala305=
ENST00000447513.7:c.855C= MANE Select	ENSP00000407922.2:p.Ala285=
ENST00000650293.1:c.809C=
ENST00000288774.7:c.915C=	ENSP00000288774.3:p.Ala305=
ENST00000447513.6:c.855C=	ENSP00000407922.2:p.Ala285=
ENST00000507596.5:c.855C=	ENSP00000424291.1:p.Ala285=
ENST00000510434.1:c.*221C=	ENSP00000423051.1:n.*221C=
NM_002617.3:c.855C=	NP_002608.1:p.Ala285=
NM_153818.1:c.915C=	NP_722540.1:p.Ala305=
XM_011541573.1:c.912C=	XP_011539875.1:p.Ala304=
XM_011541574.1:c.480C=	XP_011539876.1:p.Ala160=
XM_011541575.1:c.480C=	XP_011539877.1:p.Ala160=
XR_946666.1:n.971C=
XR_946666.2:n.920C=
NM_001374425.1:c.912C=	NP_001361354.1:p.Ala304=
NM_001374426.1:c.480C=	NP_001361355.1:p.Ala160=
NM_001374427.1:c.423C=	NP_001361356.1:p.Ala141=
NM_002617.4:c.855C= MANE Select	NP_002608.1:p.Ala285=
NM_153818.2:c.915C=	NP_722540.1:p.Ala305=
NR_164636.1:n.970C=