Canonical Allele Identifier: CA2574179477

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408879_2408880del , CM000663.2:g.2408879_2408880del	GRCh38
NC_000001.10:g.2340318_2340319del , CM000663.1:g.2340318_2340319del	GRCh37
NC_000001.9:g.2330178_2330179del	NCBI36
NG_008342.1:g.8693_8694del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.194-21_194-20del	ENSP00000288774.3:n.194-21_194-20del
ENST00000447513.7:c.194-21_194-20del MANE Select	ENSP00000407922.2:n.194-21_194-20del
ENST00000650293.1:c.148-21_148-20del
ENST00000288774.7:c.194-21_194-20del	ENSP00000288774.3:n.194-21_194-20del
ENST00000447513.6:c.194-21_194-20del	ENSP00000407922.2:n.194-21_194-20del
ENST00000502666.1:c.399-21_399-20del	ENSP00000461951.1:n.399-21_399-20del
ENST00000507596.5:c.194-21_194-20del	ENSP00000424291.1:n.194-21_194-20del
ENST00000508384.5:c.-239-21_-239-20del	ENSP00000464289.1:n.-239-21_-239-20del
ENST00000510434.1:c.194-21_194-20del	ENSP00000423051.1:n.194-21_194-20del
ENST00000514502.1:c.*211-21_*211-20del	ENSP00000425924.1:n.*211-21_*211-20del
ENST00000515760.1:n.328-21_328-20del
NM_002617.3:c.194-21_194-20del	NP_002608.1:n.194-21_194-20del
NM_153818.1:c.194-21_194-20del	NP_722540.1:n.194-21_194-20del
XM_011541573.1:c.194-21_194-20del	XP_011539875.1:n.194-21_194-20del
XM_011541574.1:c.-239-21_-239-20del	XP_011539876.1:n.-239-21_-239-20del
XM_011541575.1:c.-239-21_-239-20del	XP_011539877.1:n.-239-21_-239-20del
XM_011541576.1:c.194-21_194-20del	XP_011539878.1:n.194-21_194-20del
XR_946666.1:n.314-21_314-20del
XM_011541576.2:c.194-21_194-20del	XP_011539878.1:n.194-21_194-20del
XR_946666.2:n.263-21_263-20del
NM_001374425.1:c.194-21_194-20del	NP_001361354.1:n.194-21_194-20del
NM_001374426.1:c.-239-21_-239-20del	NP_001361355.1:n.-239-21_-239-20del
NM_001374427.1:c.-239-21_-239-20del	NP_001361356.1:n.-239-21_-239-20del
NM_002617.4:c.194-21_194-20del MANE Select	NP_002608.1:n.194-21_194-20del
NM_153818.2:c.194-21_194-20del	NP_722540.1:n.194-21_194-20del
NR_164636.1:n.313-21_313-20del