Canonical Allele Identifier: CA415775372

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337929G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406490G>A , CM000663.2:g.2406490G>A	GRCh38
NC_000001.10:g.2337929G>A , CM000663.1:g.2337929G>A	GRCh37
NC_000001.9:g.2327789G>A	NCBI36
NG_008342.1:g.11082C>T
NG_016128.1:g.19716G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.966C>T	ENSP00000288774.3:p.Ser322=
ENST00000447513.7:c.906C>T MANE Select	ENSP00000407922.2:p.Ser302=
ENST00000650293.1:c.860C>T
ENST00000288774.7:c.966C>T	ENSP00000288774.3:p.Ser322=
ENST00000447513.6:c.906C>T	ENSP00000407922.2:p.Ser302=
ENST00000507596.5:c.906C>T	ENSP00000424291.1:p.Ser302=
NM_002617.3:c.906C>T	NP_002608.1:p.Ser302=
NM_153818.1:c.966C>T	NP_722540.1:p.Ser322=
XM_011541573.1:c.963C>T	XP_011539875.1:p.Ser321=
XM_011541574.1:c.531C>T	XP_011539876.1:p.Ser177=
XM_011541575.1:c.531C>T	XP_011539877.1:p.Ser177=
XR_946666.1:n.1022C>T
XR_946666.2:n.971C>T
NM_001374425.1:c.963C>T	NP_001361354.1:p.Ser321=
NM_001374426.1:c.531C>T	NP_001361355.1:p.Ser177=
NM_001374427.1:c.474C>T	NP_001361356.1:p.Ser158=
NM_002617.4:c.906C>T MANE Select	NP_002608.1:p.Ser302=
NM_153818.2:c.966C>T	NP_722540.1:p.Ser322=
NR_164636.1:n.1021C>T