Canonical Allele Identifier: CA337984109

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337942G>A (hg19) ; chr1:g.2406503G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406503G>A , CM000663.2:g.2406503G>A	GRCh38
NC_000001.10:g.2337942G>A , CM000663.1:g.2337942G>A	GRCh37
NC_000001.9:g.2327802G>A	NCBI36
NG_008342.1:g.11069C>T
NG_016128.1:g.19729G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.953C>T	ENSP00000288774.3:p.Thr318Ile
ENST00000447513.7:c.893C>T MANE Select	ENSP00000407922.2:p.Thr298Ile
ENST00000650293.1:c.847C>T
ENST00000288774.7:c.953C>T	ENSP00000288774.3:p.Thr318Ile
ENST00000447513.6:c.893C>T	ENSP00000407922.2:p.Thr298Ile
ENST00000507596.5:c.893C>T	ENSP00000424291.1:p.Thr298Ile
NM_002617.3:c.893C>T	NP_002608.1:p.Thr298Ile
NM_153818.1:c.953C>T	NP_722540.1:p.Thr318Ile
XM_011541573.1:c.950C>T	XP_011539875.1:p.Thr317Ile
XM_011541574.1:c.518C>T	XP_011539876.1:p.Thr173Ile
XM_011541575.1:c.518C>T	XP_011539877.1:p.Thr173Ile
XR_946666.1:n.1009C>T
XR_946666.2:n.958C>T
NM_001374425.1:c.950C>T	NP_001361354.1:p.Thr317Ile
NM_001374426.1:c.518C>T	NP_001361355.1:p.Thr173Ile
NM_001374427.1:c.461C>T	NP_001361356.1:p.Thr154Ile
NM_002617.4:c.893C>T MANE Select	NP_002608.1:p.Thr298Ile
NM_153818.2:c.953C>T	NP_722540.1:p.Thr318Ile
NR_164636.1:n.1008C>T