Canonical Allele Identifier: CA337984201

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337957C>G (hg19) ; chr1:g.2406518C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406518C>G , CM000663.2:g.2406518C>G	GRCh38
NC_000001.10:g.2337957C>G , CM000663.1:g.2337957C>G	GRCh37
NC_000001.9:g.2327817C>G	NCBI36
NG_008342.1:g.11054G>C
NG_016128.1:g.19744C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.938G>C	ENSP00000288774.3:p.Cys313Ser
ENST00000447513.7:c.878G>C MANE Select	ENSP00000407922.2:p.Cys293Ser
ENST00000650293.1:c.832G>C
ENST00000288774.7:c.938G>C	ENSP00000288774.3:p.Cys313Ser
ENST00000447513.6:c.878G>C	ENSP00000407922.2:p.Cys293Ser
ENST00000507596.5:c.878G>C	ENSP00000424291.1:p.Cys293Ser
ENST00000510434.1:c.*244G>C	ENSP00000423051.1:n.*244G>C
NM_002617.3:c.878G>C	NP_002608.1:p.Cys293Ser
NM_153818.1:c.938G>C	NP_722540.1:p.Cys313Ser
XM_011541573.1:c.935G>C	XP_011539875.1:p.Cys312Ser
XM_011541574.1:c.503G>C	XP_011539876.1:p.Cys168Ser
XM_011541575.1:c.503G>C	XP_011539877.1:p.Cys168Ser
XR_946666.1:n.994G>C
XR_946666.2:n.943G>C
NM_001374425.1:c.935G>C	NP_001361354.1:p.Cys312Ser
NM_001374426.1:c.503G>C	NP_001361355.1:p.Cys168Ser
NM_001374427.1:c.446G>C	NP_001361356.1:p.Cys149Ser
NM_002617.4:c.878G>C MANE Select	NP_002608.1:p.Cys293Ser
NM_153818.2:c.938G>C	NP_722540.1:p.Cys313Ser
NR_164636.1:n.993G>C