Canonical Allele Identifier: CA2742186757

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408943_2408947del , CM000663.2:g.2408943_2408947del	GRCh38
NC_000001.10:g.2340382_2340386del , CM000663.1:g.2340382_2340386del	GRCh37
NC_000001.9:g.2330242_2330246del	NCBI36
NG_008342.1:g.8625_8629del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.194-89_194-85del	ENSP00000288774.3:n.194-89_194-85del
ENST00000447513.7:c.194-89_194-85del MANE Select	ENSP00000407922.2:n.194-89_194-85del
ENST00000650293.1:c.148-89_148-85del
ENST00000288774.7:c.194-89_194-85del	ENSP00000288774.3:n.194-89_194-85del
ENST00000447513.6:c.194-89_194-85del	ENSP00000407922.2:n.194-89_194-85del
ENST00000502666.1:c.399-89_399-85del	ENSP00000461951.1:n.399-89_399-85del
ENST00000507596.5:c.194-89_194-85del	ENSP00000424291.1:n.194-89_194-85del
ENST00000508384.5:c.-239-89_-239-85del	ENSP00000464289.1:n.-239-89_-239-85del
ENST00000510434.1:c.194-89_194-85del	ENSP00000423051.1:n.194-89_194-85del
ENST00000514502.1:c.*211-89_*211-85del	ENSP00000425924.1:n.*211-89_*211-85del
ENST00000515760.1:n.328-89_328-85del
NM_002617.3:c.194-89_194-85del	NP_002608.1:n.194-89_194-85del
NM_153818.1:c.194-89_194-85del	NP_722540.1:n.194-89_194-85del
XM_011541573.1:c.194-89_194-85del	XP_011539875.1:n.194-89_194-85del
XM_011541574.1:c.-239-89_-239-85del	XP_011539876.1:n.-239-89_-239-85del
XM_011541575.1:c.-239-89_-239-85del	XP_011539877.1:n.-239-89_-239-85del
XM_011541576.1:c.194-89_194-85del	XP_011539878.1:n.194-89_194-85del
XR_946666.1:n.314-89_314-85del
XM_011541576.2:c.194-89_194-85del	XP_011539878.1:n.194-89_194-85del
XR_946666.2:n.263-89_263-85del
NM_001374425.1:c.194-89_194-85del	NP_001361354.1:n.194-89_194-85del
NM_001374426.1:c.-239-89_-239-85del	NP_001361355.1:n.-239-89_-239-85del
NM_001374427.1:c.-239-89_-239-85del	NP_001361356.1:n.-239-89_-239-85del
NM_002617.4:c.194-89_194-85del MANE Select	NP_002608.1:n.194-89_194-85del
NM_153818.2:c.194-89_194-85del	NP_722540.1:n.194-89_194-85del
NR_164636.1:n.313-89_313-85del