Canonical Allele Identifier: CA337984124

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337943T>C (hg19) ; chr1:g.2406504T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406504T>C , CM000663.2:g.2406504T>C	GRCh38
NC_000001.10:g.2337943T>C , CM000663.1:g.2337943T>C	GRCh37
NC_000001.9:g.2327803T>C	NCBI36
NG_008342.1:g.11068A>G
NG_016128.1:g.19730T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.952A>G	ENSP00000288774.3:p.Thr318Ala
ENST00000447513.7:c.892A>G MANE Select	ENSP00000407922.2:p.Thr298Ala
ENST00000650293.1:c.846A>G
ENST00000288774.7:c.952A>G	ENSP00000288774.3:p.Thr318Ala
ENST00000447513.6:c.892A>G	ENSP00000407922.2:p.Thr298Ala
ENST00000507596.5:c.892A>G	ENSP00000424291.1:p.Thr298Ala
NM_002617.3:c.892A>G	NP_002608.1:p.Thr298Ala
NM_153818.1:c.952A>G	NP_722540.1:p.Thr318Ala
XM_011541573.1:c.949A>G	XP_011539875.1:p.Thr317Ala
XM_011541574.1:c.517A>G	XP_011539876.1:p.Thr173Ala
XM_011541575.1:c.517A>G	XP_011539877.1:p.Thr173Ala
XR_946666.1:n.1008A>G
XR_946666.2:n.957A>G
NM_001374425.1:c.949A>G	NP_001361354.1:p.Thr317Ala
NM_001374426.1:c.517A>G	NP_001361355.1:p.Thr173Ala
NM_001374427.1:c.460A>G	NP_001361356.1:p.Thr154Ala
NM_002617.4:c.892A>G MANE Select	NP_002608.1:p.Thr298Ala
NM_153818.2:c.952A>G	NP_722540.1:p.Thr318Ala
NR_164636.1:n.1007A>G