Canonical Allele Identifier: CA1149571909

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408761_2408762delinsTG , CM000663.2:g.2408761_2408762delinsTG	GRCh38
NC_000001.10:g.2340200_2340201delinsTG , CM000663.1:g.2340200_2340201delinsTG	GRCh37
NC_000001.9:g.2330060_2330061delinsTG	NCBI36
NG_008342.1:g.8810_8811delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.290_291delinsCA	ENSP00000288774.3:p.Thr97=
ENST00000447513.7:c.290_291delinsCA MANE Select	ENSP00000407922.2:p.Thr97=
ENST00000650293.1:c.244_245delinsCA
ENST00000288774.7:c.290_291delinsCA	ENSP00000288774.3:p.Thr97=
ENST00000447513.6:c.290_291delinsCA	ENSP00000407922.2:p.Thr97=
ENST00000502666.1:c.495_496delinsCA	ENSP00000461951.1:n.495_496delinsCA
ENST00000507596.5:c.290_291delinsCA	ENSP00000424291.1:p.Thr97=
ENST00000508384.5:c.-143_-142delinsCA	ENSP00000464289.1:n.-143_-142delinsCA
ENST00000510434.1:c.290_291delinsCA	ENSP00000423051.1:p.Thr97=
ENST00000514502.1:c.*307_*308delinsCA	ENSP00000425924.1:n.*307_*308delinsCA
ENST00000515760.1:n.424_425delinsCA
NM_002617.3:c.290_291delinsCA	NP_002608.1:p.Thr97=
NM_153818.1:c.290_291delinsCA	NP_722540.1:p.Thr97=
XM_011541573.1:c.290_291delinsCA	XP_011539875.1:p.Thr97=
XM_011541574.1:c.-143_-142delinsCA	XP_011539876.1:n.-143_-142delinsCA
XM_011541575.1:c.-143_-142delinsCA	XP_011539877.1:n.-143_-142delinsCA
XM_011541576.1:c.290_291delinsCA	XP_011539878.1:p.Thr97=
XR_946666.1:n.410_411delinsCA
XM_011541576.2:c.290_291delinsCA	XP_011539878.1:p.Thr97=
XR_946666.2:n.359_360delinsCA
NM_001374425.1:c.290_291delinsCA	NP_001361354.1:p.Thr97=
NM_001374426.1:c.-143_-142delinsCA	NP_001361355.1:n.-143_-142delinsCA
NM_001374427.1:c.-143_-142delinsCA	NP_001361356.1:n.-143_-142delinsCA
NM_002617.4:c.290_291delinsCA MANE Select	NP_002608.1:p.Thr97=
NM_153818.2:c.290_291delinsCA	NP_722540.1:p.Thr97=
NR_164636.1:n.409_410delinsCA