Canonical Allele Identifier: CA358179

Gene: PEX10

Linked Data

• ClinVar Variation Id: 225040
• ClinVar RCV Id: RCV000210672 ; RCV002515587
• dbSNP Id: rs869312935
• gnomAD v4: 1-2406719-C-G
• MyVariant Identifiers: chr1:g.2338158C>G (hg19) ; chr1:g.2406719C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406719C>G , CM000663.2:g.2406719C>G	GRCh38
NC_000001.10:g.2338158C>G , CM000663.1:g.2338158C>G	GRCh37
NC_000001.9:g.2328018C>G	NCBI36
NG_008342.1:g.10853G>C
NG_016128.1:g.19945C>G

Transcript Alleles

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