Canonical Allele Identifier: CA337984300

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337973A>T (hg19) ; chr1:g.2406534A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406534A>T , CM000663.2:g.2406534A>T	GRCh38
NC_000001.10:g.2337973A>T , CM000663.1:g.2337973A>T	GRCh37
NC_000001.9:g.2327833A>T	NCBI36
NG_008342.1:g.11038T>A
NG_016128.1:g.19760A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.922T>A	ENSP00000288774.3:p.Cys308Ser
ENST00000447513.7:c.862T>A MANE Select	ENSP00000407922.2:p.Cys288Ser
ENST00000650293.1:c.816T>A
ENST00000288774.7:c.922T>A	ENSP00000288774.3:p.Cys308Ser
ENST00000447513.6:c.862T>A	ENSP00000407922.2:p.Cys288Ser
ENST00000507596.5:c.862T>A	ENSP00000424291.1:p.Cys288Ser
ENST00000510434.1:c.*228T>A	ENSP00000423051.1:n.*228T>A
NM_002617.3:c.862T>A	NP_002608.1:p.Cys288Ser
NM_153818.1:c.922T>A	NP_722540.1:p.Cys308Ser
XM_011541573.1:c.919T>A	XP_011539875.1:p.Cys307Ser
XM_011541574.1:c.487T>A	XP_011539876.1:p.Cys163Ser
XM_011541575.1:c.487T>A	XP_011539877.1:p.Cys163Ser
XR_946666.1:n.978T>A
XR_946666.2:n.927T>A
NM_001374425.1:c.919T>A	NP_001361354.1:p.Cys307Ser
NM_001374426.1:c.487T>A	NP_001361355.1:p.Cys163Ser
NM_001374427.1:c.430T>A	NP_001361356.1:p.Cys144Ser
NM_002617.4:c.862T>A MANE Select	NP_002608.1:p.Cys288Ser
NM_153818.2:c.922T>A	NP_722540.1:p.Cys308Ser
NR_164636.1:n.977T>A