Canonical Allele Identifier: CA415776118

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2340083A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408644A>G , CM000663.2:g.2408644A>G	GRCh38
NC_000001.10:g.2340083A>G , CM000663.1:g.2340083A>G	GRCh37
NC_000001.9:g.2329943A>G	NCBI36
NG_008342.1:g.8928T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.408T>C	ENSP00000288774.3:p.Arg136=
ENST00000447513.7:c.408T>C MANE Select	ENSP00000407922.2:p.Arg136=
ENST00000650293.1:c.362T>C
ENST00000288774.7:c.408T>C	ENSP00000288774.3:p.Arg136=
ENST00000447513.6:c.408T>C	ENSP00000407922.2:p.Arg136=
ENST00000502666.1:c.613T>C	ENSP00000461951.1:n.613T>C
ENST00000507596.5:c.408T>C	ENSP00000424291.1:p.Arg136=
ENST00000508384.5:c.-25T>C	ENSP00000464289.1:n.-25T>C
ENST00000510434.1:c.408T>C	ENSP00000423051.1:p.Arg136=
ENST00000515760.1:n.542T>C
NM_002617.3:c.408T>C	NP_002608.1:p.Arg136=
NM_153818.1:c.408T>C	NP_722540.1:p.Arg136=
XM_011541573.1:c.408T>C	XP_011539875.1:p.Arg136=
XM_011541574.1:c.-25T>C	XP_011539876.1:n.-25T>C
XM_011541575.1:c.-25T>C	XP_011539877.1:n.-25T>C
XM_011541576.1:c.408T>C	XP_011539878.1:p.Arg136=
XR_946666.1:n.528T>C
XM_011541576.2:c.408T>C	XP_011539878.1:p.Arg136=
XR_946666.2:n.477T>C
NM_001374425.1:c.408T>C	NP_001361354.1:p.Arg136=
NM_001374426.1:c.-25T>C	NP_001361355.1:n.-25T>C
NM_001374427.1:c.-25T>C	NP_001361356.1:n.-25T>C
NM_002617.4:c.408T>C MANE Select	NP_002608.1:p.Arg136=
NM_153818.2:c.408T>C	NP_722540.1:p.Arg136=
NR_164636.1:n.527T>C