Canonical Allele Identifier: CA538228

Gene: PEX10

Linked Data

• ClinVar Variation Id: 1409192
• ClinVar RCV Id: RCV001909694
• dbSNP Id: rs778774616
• ExAC: 1:2340219 C / T
• gnomAD v2: 1-2340219-C-T
• gnomAD v3: 1-2408780-C-T
• gnomAD v4: 1-2408780-C-T
• MyVariant Identifiers: chr1:g.2340219C>T (hg19) ; chr1:g.2408780C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408780C>T , CM000663.2:g.2408780C>T	GRCh38
NC_000001.10:g.2340219C>T , CM000663.1:g.2340219C>T	GRCh37
NC_000001.9:g.2330079C>T	NCBI36
NG_008342.1:g.8792G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000288774.8:c.272G>A	ENSP00000288774.3:p.Arg91His
ENST00000447513.7:c.272G>A MANE Select	ENSP00000407922.2:p.Arg91His
ENST00000650293.1:c.226G>A
ENST00000288774.7:c.272G>A	ENSP00000288774.3:p.Arg91His
ENST00000447513.6:c.272G>A	ENSP00000407922.2:p.Arg91His
ENST00000502666.1:c.477G>A	ENSP00000461951.1:n.477G>A
ENST00000507596.5:c.272G>A	ENSP00000424291.1:p.Arg91His
ENST00000508384.5:c.-161G>A	ENSP00000464289.1:n.-161G>A
ENST00000510434.1:c.272G>A	ENSP00000423051.1:p.Arg91His
ENST00000514502.1:c.*289G>A	ENSP00000425924.1:n.*289G>A
ENST00000515760.1:n.406G>A
NM_002617.3:c.272G>A	NP_002608.1:p.Arg91His
NM_153818.1:c.272G>A	NP_722540.1:p.Arg91His
XM_011541573.1:c.272G>A	XP_011539875.1:p.Arg91His
XM_011541574.1:c.-161G>A	XP_011539876.1:n.-161G>A
XM_011541575.1:c.-161G>A	XP_011539877.1:n.-161G>A
XM_011541576.1:c.272G>A	XP_011539878.1:p.Arg91His
XR_946666.1:n.392G>A
XM_011541576.2:c.272G>A	XP_011539878.1:p.Arg91His
XR_946666.2:n.341G>A
NM_001374425.1:c.272G>A	NP_001361354.1:p.Arg91His
NM_001374426.1:c.-161G>A	NP_001361355.1:n.-161G>A
NM_001374427.1:c.-161G>A	NP_001361356.1:n.-161G>A
NM_002617.4:c.272G>A MANE Select	NP_002608.1:p.Arg91His
NM_153818.2:c.272G>A	NP_722540.1:p.Arg91His
NR_164636.1:n.391G>A