Canonical Allele Identifier: CA337984058

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337933C>A (hg19) ; chr1:g.2406494C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406494C>A , CM000663.2:g.2406494C>A	GRCh38
NC_000001.10:g.2337933C>A , CM000663.1:g.2337933C>A	GRCh37
NC_000001.9:g.2327793C>A	NCBI36
NG_008342.1:g.11078G>T
NG_016128.1:g.19720C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.962G>T	ENSP00000288774.3:p.Cys321Phe
ENST00000447513.7:c.902G>T MANE Select	ENSP00000407922.2:p.Cys301Phe
ENST00000650293.1:c.856G>T
ENST00000288774.7:c.962G>T	ENSP00000288774.3:p.Cys321Phe
ENST00000447513.6:c.902G>T	ENSP00000407922.2:p.Cys301Phe
ENST00000507596.5:c.902G>T	ENSP00000424291.1:p.Cys301Phe
NM_002617.3:c.902G>T	NP_002608.1:p.Cys301Phe
NM_153818.1:c.962G>T	NP_722540.1:p.Cys321Phe
XM_011541573.1:c.959G>T	XP_011539875.1:p.Cys320Phe
XM_011541574.1:c.527G>T	XP_011539876.1:p.Cys176Phe
XM_011541575.1:c.527G>T	XP_011539877.1:p.Cys176Phe
XR_946666.1:n.1018G>T
XR_946666.2:n.967G>T
NM_001374425.1:c.959G>T	NP_001361354.1:p.Cys320Phe
NM_001374426.1:c.527G>T	NP_001361355.1:p.Cys176Phe
NM_001374427.1:c.470G>T	NP_001361356.1:p.Cys157Phe
NM_002617.4:c.902G>T MANE Select	NP_002608.1:p.Cys301Phe
NM_153818.2:c.962G>T	NP_722540.1:p.Cys321Phe
NR_164636.1:n.1017G>T