Canonical Allele Identifier: CA1149571876

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408691_2408695delinsGGTCA , CM000663.2:g.2408691_2408695delinsGGTCA	GRCh38
NC_000001.10:g.2340130_2340134delinsGGTCA , CM000663.1:g.2340130_2340134delinsGGTCA	GRCh37
NC_000001.9:g.2329990_2329994delinsGGTCA	NCBI36
NG_008342.1:g.8877_8881delinsTGACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.357_361delinsTGACC	ENSP00000288774.3:p.Ala119=
ENST00000447513.7:c.357_361delinsTGACC MANE Select	ENSP00000407922.2:p.Ala119=
ENST00000650293.1:c.311_315delinsTGACC
ENST00000288774.7:c.357_361delinsTGACC	ENSP00000288774.3:p.Ala119=
ENST00000447513.6:c.357_361delinsTGACC	ENSP00000407922.2:p.Ala119=
ENST00000502666.1:c.562_566delinsTGACC	ENSP00000461951.1:n.562_566delinsTGACC
ENST00000507596.5:c.357_361delinsTGACC	ENSP00000424291.1:p.Ala119=
ENST00000508384.5:c.-76_-72delinsTGACC	ENSP00000464289.1:n.-76_-72delinsTGACC
ENST00000510434.1:c.357_361delinsTGACC	ENSP00000423051.1:p.Ala119=
ENST00000515760.1:n.491_495delinsTGACC
NM_002617.3:c.357_361delinsTGACC	NP_002608.1:p.Ala119=
NM_153818.1:c.357_361delinsTGACC	NP_722540.1:p.Ala119=
XM_011541573.1:c.357_361delinsTGACC	XP_011539875.1:p.Ala119=
XM_011541574.1:c.-76_-72delinsTGACC	XP_011539876.1:n.-76_-72delinsTGACC
XM_011541575.1:c.-76_-72delinsTGACC	XP_011539877.1:n.-76_-72delinsTGACC
XM_011541576.1:c.357_361delinsTGACC	XP_011539878.1:p.Ala119=
XR_946666.1:n.477_481delinsTGACC
XM_011541576.2:c.357_361delinsTGACC	XP_011539878.1:p.Ala119=
XR_946666.2:n.426_430delinsTGACC
NM_001374425.1:c.357_361delinsTGACC	NP_001361354.1:p.Ala119=
NM_001374426.1:c.-76_-72delinsTGACC	NP_001361355.1:n.-76_-72delinsTGACC
NM_001374427.1:c.-76_-72delinsTGACC	NP_001361356.1:n.-76_-72delinsTGACC
NM_002617.4:c.357_361delinsTGACC MANE Select	NP_002608.1:p.Ala119=
NM_153818.2:c.357_361delinsTGACC	NP_722540.1:p.Ala119=
NR_164636.1:n.476_480delinsTGACC