Canonical Allele Identifier: CA337984538

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406576T>A , CM000663.2:g.2406576T>A	GRCh38
NC_000001.10:g.2338015T>A , CM000663.1:g.2338015T>A	GRCh37
NC_000001.9:g.2327875T>A	NCBI36
NG_008342.1:g.10996A>T
NG_016128.1:g.19802T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.880A>T	ENSP00000288774.3:p.Thr294Ser
ENST00000447513.7:c.820A>T MANE Select	ENSP00000407922.2:p.Thr274Ser
ENST00000650293.1:c.774A>T
ENST00000288774.7:c.880A>T	ENSP00000288774.3:p.Thr294Ser
ENST00000447513.6:c.820A>T	ENSP00000407922.2:p.Thr274Ser
ENST00000507596.5:c.820A>T	ENSP00000424291.1:p.Thr274Ser
ENST00000510434.1:c.*186A>T	ENSP00000423051.1:n.*186A>T
NM_002617.3:c.820A>T	NP_002608.1:p.Thr274Ser
NM_153818.1:c.880A>T	NP_722540.1:p.Thr294Ser
XM_011541573.1:c.877A>T	XP_011539875.1:p.Thr293Ser
XM_011541574.1:c.445A>T	XP_011539876.1:p.Thr149Ser
XM_011541575.1:c.445A>T	XP_011539877.1:p.Thr149Ser
XR_946666.1:n.936A>T
XR_946666.2:n.885A>T
NM_001374425.1:c.877A>T	NP_001361354.1:p.Thr293Ser
NM_001374426.1:c.445A>T	NP_001361355.1:p.Thr149Ser
NM_001374427.1:c.388A>T	NP_001361356.1:p.Thr130Ser
NM_002617.4:c.820A>T MANE Select	NP_002608.1:p.Thr274Ser
NM_153818.2:c.880A>T	NP_722540.1:p.Thr294Ser
NR_164636.1:n.935A>T