Canonical Allele Identifier: CA337984528

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406575G>C , CM000663.2:g.2406575G>C	GRCh38
NC_000001.10:g.2338014G>C , CM000663.1:g.2338014G>C	GRCh37
NC_000001.9:g.2327874G>C	NCBI36
NG_008342.1:g.10997C>G
NG_016128.1:g.19801G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.881C>G	ENSP00000288774.3:p.Thr294Ser
ENST00000447513.7:c.821C>G MANE Select	ENSP00000407922.2:p.Thr274Ser
ENST00000650293.1:c.775C>G
ENST00000288774.7:c.881C>G	ENSP00000288774.3:p.Thr294Ser
ENST00000447513.6:c.821C>G	ENSP00000407922.2:p.Thr274Ser
ENST00000507596.5:c.821C>G	ENSP00000424291.1:p.Thr274Ser
ENST00000510434.1:c.*187C>G	ENSP00000423051.1:n.*187C>G
NM_002617.3:c.821C>G	NP_002608.1:p.Thr274Ser
NM_153818.1:c.881C>G	NP_722540.1:p.Thr294Ser
XM_011541573.1:c.878C>G	XP_011539875.1:p.Thr293Ser
XM_011541574.1:c.446C>G	XP_011539876.1:p.Thr149Ser
XM_011541575.1:c.446C>G	XP_011539877.1:p.Thr149Ser
XR_946666.1:n.937C>G
XR_946666.2:n.886C>G
NM_001374425.1:c.878C>G	NP_001361354.1:p.Thr293Ser
NM_001374426.1:c.446C>G	NP_001361355.1:p.Thr149Ser
NM_001374427.1:c.389C>G	NP_001361356.1:p.Thr130Ser
NM_002617.4:c.821C>G MANE Select	NP_002608.1:p.Thr274Ser
NM_153818.2:c.881C>G	NP_722540.1:p.Thr294Ser
NR_164636.1:n.936C>G