Canonical Allele Identifier: CA337984199

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337956G>T (hg19) ; chr1:g.2406517G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406517G>T , CM000663.2:g.2406517G>T	GRCh38
NC_000001.10:g.2337956G>T , CM000663.1:g.2337956G>T	GRCh37
NC_000001.9:g.2327816G>T	NCBI36
NG_008342.1:g.11055C>A
NG_016128.1:g.19743G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.939C>A	ENSP00000288774.3:p.Cys313Ter
ENST00000447513.7:c.879C>A MANE Select	ENSP00000407922.2:p.Cys293Ter
ENST00000650293.1:c.833C>A
ENST00000288774.7:c.939C>A	ENSP00000288774.3:p.Cys313Ter
ENST00000447513.6:c.879C>A	ENSP00000407922.2:p.Cys293Ter
ENST00000507596.5:c.879C>A	ENSP00000424291.1:p.Cys293Ter
NM_002617.3:c.879C>A	NP_002608.1:p.Cys293Ter
NM_153818.1:c.939C>A	NP_722540.1:p.Cys313Ter
XM_011541573.1:c.936C>A	XP_011539875.1:p.Cys312Ter
XM_011541574.1:c.504C>A	XP_011539876.1:p.Cys168Ter
XM_011541575.1:c.504C>A	XP_011539877.1:p.Cys168Ter
XR_946666.1:n.995C>A
XR_946666.2:n.944C>A
NM_001374425.1:c.936C>A	NP_001361354.1:p.Cys312Ter
NM_001374426.1:c.504C>A	NP_001361355.1:p.Cys168Ter
NM_001374427.1:c.447C>A	NP_001361356.1:p.Cys149Ter
NM_002617.4:c.879C>A MANE Select	NP_002608.1:p.Cys293Ter
NM_153818.2:c.939C>A	NP_722540.1:p.Cys313Ter
NR_164636.1:n.994C>A