Canonical Allele Identifier: CA337984048

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337931T>A (hg19) ; chr1:g.2406492T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406492T>A , CM000663.2:g.2406492T>A	GRCh38
NC_000001.10:g.2337931T>A , CM000663.1:g.2337931T>A	GRCh37
NC_000001.9:g.2327791T>A	NCBI36
NG_008342.1:g.11080A>T
NG_016128.1:g.19718T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.964A>T	ENSP00000288774.3:p.Ser322Cys
ENST00000447513.7:c.904A>T MANE Select	ENSP00000407922.2:p.Ser302Cys
ENST00000650293.1:c.858A>T
ENST00000288774.7:c.964A>T	ENSP00000288774.3:p.Ser322Cys
ENST00000447513.6:c.904A>T	ENSP00000407922.2:p.Ser302Cys
ENST00000507596.5:c.904A>T	ENSP00000424291.1:p.Ser302Cys
NM_002617.3:c.904A>T	NP_002608.1:p.Ser302Cys
NM_153818.1:c.964A>T	NP_722540.1:p.Ser322Cys
XM_011541573.1:c.961A>T	XP_011539875.1:p.Ser321Cys
XM_011541574.1:c.529A>T	XP_011539876.1:p.Ser177Cys
XM_011541575.1:c.529A>T	XP_011539877.1:p.Ser177Cys
XR_946666.1:n.1020A>T
XR_946666.2:n.969A>T
NM_001374425.1:c.961A>T	NP_001361354.1:p.Ser321Cys
NM_001374426.1:c.529A>T	NP_001361355.1:p.Ser177Cys
NM_001374427.1:c.472A>T	NP_001361356.1:p.Ser158Cys
NM_002617.4:c.904A>T MANE Select	NP_002608.1:p.Ser302Cys
NM_153818.2:c.964A>T	NP_722540.1:p.Ser322Cys
NR_164636.1:n.1019A>T