Canonical Allele Identifier: CA521014070

Gene: PEX10

Linked Data

• dbSNP Id: rs1372612395
• gnomAD v2: 1-2338143-T-C
• gnomAD v4: 1-2406704-T-C
• MyVariant Identifiers: chr1:g.2338143T>C (hg19) ; chr1:g.2406704T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406704T>C , CM000663.2:g.2406704T>C	GRCh38
NC_000001.10:g.2338143T>C , CM000663.1:g.2338143T>C	GRCh37
NC_000001.9:g.2328003T>C	NCBI36
NG_008342.1:g.10868A>G
NG_016128.1:g.19930T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.836+16A>G	ENSP00000288774.3:n.836+16A>G
ENST00000447513.7:c.776+16A>G MANE Select	ENSP00000407922.2:n.776+16A>G
ENST00000650293.1:c.730+16A>G
ENST00000288774.7:c.836+16A>G	ENSP00000288774.3:n.836+16A>G
ENST00000447513.6:c.776+16A>G	ENSP00000407922.2:n.776+16A>G
ENST00000507596.5:c.776+16A>G	ENSP00000424291.1:n.776+16A>G
ENST00000510434.1:c.*142+16A>G	ENSP00000423051.1:n.*142+16A>G
NM_002617.3:c.776+16A>G	NP_002608.1:n.776+16A>G
NM_153818.1:c.836+16A>G	NP_722540.1:n.836+16A>G
XM_011541573.1:c.833+16A>G	XP_011539875.1:n.833+16A>G
XM_011541574.1:c.401+16A>G	XP_011539876.1:n.401+16A>G
XM_011541575.1:c.401+16A>G	XP_011539877.1:n.401+16A>G
XR_946666.1:n.892+16A>G
XR_946666.2:n.841+16A>G
NM_001374425.1:c.833+16A>G	NP_001361354.1:n.833+16A>G
NM_001374426.1:c.401+16A>G	NP_001361355.1:n.401+16A>G
NM_001374427.1:c.344+16A>G	NP_001361356.1:n.344+16A>G
NM_002617.4:c.776+16A>G MANE Select	NP_002608.1:n.776+16A>G
NM_153818.2:c.836+16A>G	NP_722540.1:n.836+16A>G
NR_164636.1:n.891+16A>G