Canonical Allele Identifier: CA415775724

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2339975G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408536G>T , CM000663.2:g.2408536G>T	GRCh38
NC_000001.10:g.2339975G>T , CM000663.1:g.2339975G>T	GRCh37
NC_000001.9:g.2329835G>T	NCBI36
NG_008342.1:g.9036C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.516C>A	ENSP00000288774.3:p.Ala172=
ENST00000447513.7:c.516C>A MANE Select	ENSP00000407922.2:p.Ala172=
ENST00000650293.1:c.470C>A
ENST00000288774.7:c.516C>A	ENSP00000288774.3:p.Ala172=
ENST00000447513.6:c.516C>A	ENSP00000407922.2:p.Ala172=
ENST00000507596.5:c.516C>A	ENSP00000424291.1:p.Ala172=
ENST00000508384.5:c.84C>A	ENSP00000464289.1:p.Ala28=
ENST00000510434.1:c.516C>A	ENSP00000423051.1:p.Ala172=
NM_002617.3:c.516C>A	NP_002608.1:p.Ala172=
NM_153818.1:c.516C>A	NP_722540.1:p.Ala172=
XM_011541573.1:c.516C>A	XP_011539875.1:p.Ala172=
XM_011541574.1:c.84C>A	XP_011539876.1:p.Ala28=
XM_011541575.1:c.84C>A	XP_011539877.1:p.Ala28=
XM_011541576.1:c.516C>A	XP_011539878.1:p.Ala172=
XR_946666.1:n.636C>A
XM_011541576.2:c.516C>A	XP_011539878.1:p.Ala172=
XR_946666.2:n.585C>A
NM_001374425.1:c.516C>A	NP_001361354.1:p.Ala172=
NM_001374426.1:c.84C>A	NP_001361355.1:p.Ala28=
NM_001374427.1:c.84C>A	NP_001361356.1:p.Ala28=
NM_002617.4:c.516C>A MANE Select	NP_002608.1:p.Ala172=
NM_153818.2:c.516C>A	NP_722540.1:p.Ala172=
NR_164636.1:n.635C>A