Canonical Allele Identifier: CA10610815

Gene: PEX10

Linked Data

• ClinVar Variation Id: 296269
• ClinVar RCV Id: RCV000386410
• dbSNP Id: rs886046145
• MyVariant Identifiers: chr1:g.2337114T>C (hg19) ; chr1:g.2405675T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2405675T>C , CM000663.2:g.2405675T>C	GRCh38
NC_000001.10:g.2337114T>C , CM000663.1:g.2337114T>C	GRCh37
NC_000001.9:g.2326974T>C	NCBI36
NG_008342.1:g.11897A>G
NG_016128.1:g.18901T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.*91A>G	ENSP00000288774.3:n.*91A>G
ENST00000447513.7:c.*91A>G MANE Select	ENSP00000407922.2:n.*91A>G
ENST00000650293.1:c.1026A>G
ENST00000288774.7:c.*91A>G	ENSP00000288774.3:n.*91A>G
ENST00000447513.6:c.*91A>G	ENSP00000407922.2:n.*91A>G
ENST00000507596.5:c.*91A>G	ENSP00000424291.1:n.*91A>G
NM_002617.3:c.*91A>G	NP_002608.1:n.*91A>G
NM_153818.1:c.*91A>G	NP_722540.1:n.*91A>G
XM_011541573.1:c.*91A>G	XP_011539875.1:n.*91A>G
XM_011541574.1:c.*91A>G	XP_011539876.1:n.*91A>G
XM_011541575.1:c.*91A>G	XP_011539877.1:n.*91A>G
XR_946666.1:n.1188A>G
XR_946666.2:n.1137A>G
NM_001374425.1:c.*91A>G	NP_001361354.1:n.*91A>G
NM_001374426.1:c.*91A>G	NP_001361355.1:n.*91A>G
NM_001374427.1:c.*91A>G	NP_001361356.1:n.*91A>G
NM_002617.4:c.*91A>G MANE Select	NP_002608.1:n.*91A>G
NM_153818.2:c.*91A>G	NP_722540.1:n.*91A>G
NR_164636.1:n.1187A>G