Canonical Allele Identifier: CA2697552030

Gene: PEX10

Linked Data

• ClinVar Variation Id: 2707617
• ClinVar RCV Id: RCV003536451

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406706del , CM000663.2:g.2406706del	GRCh38
NC_000001.10:g.2338145del , CM000663.1:g.2338145del	GRCh37
NC_000001.9:g.2328005del	NCBI36
NG_008342.1:g.10867del
NG_016128.1:g.19932del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.836+15del	ENSP00000288774.3:n.836+15del
ENST00000447513.7:c.776+15del MANE Select	ENSP00000407922.2:n.776+15del
ENST00000650293.1:c.730+15del
ENST00000288774.7:c.836+15del	ENSP00000288774.3:n.836+15del
ENST00000447513.6:c.776+15del	ENSP00000407922.2:n.776+15del
ENST00000507596.5:c.776+15del	ENSP00000424291.1:n.776+15del
ENST00000510434.1:c.*142+15del	ENSP00000423051.1:n.*142+15del
NM_002617.3:c.776+15del	NP_002608.1:n.776+15del
NM_153818.1:c.836+15del	NP_722540.1:n.836+15del
XM_011541573.1:c.833+15del	XP_011539875.1:n.833+15del
XM_011541574.1:c.401+15del	XP_011539876.1:n.401+15del
XM_011541575.1:c.401+15del	XP_011539877.1:n.401+15del
XR_946666.1:n.892+15del
XR_946666.2:n.841+15del
NM_001374425.1:c.833+15del	NP_001361354.1:n.833+15del
NM_001374426.1:c.401+15del	NP_001361355.1:n.401+15del
NM_001374427.1:c.344+15del	NP_001361356.1:n.344+15del
NM_002617.4:c.776+15del MANE Select	NP_002608.1:n.776+15del
NM_153818.2:c.836+15del	NP_722540.1:n.836+15del
NR_164636.1:n.891+15del