Canonical Allele Identifier: CA337987788

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2340049G>A (hg19) ; chr1:g.2408610G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408610G>A , CM000663.2:g.2408610G>A	GRCh38
NC_000001.10:g.2340049G>A , CM000663.1:g.2340049G>A	GRCh37
NC_000001.9:g.2329909G>A	NCBI36
NG_008342.1:g.8962C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.442C>T	ENSP00000288774.3:p.His148Tyr
ENST00000447513.7:c.442C>T MANE Select	ENSP00000407922.2:p.His148Tyr
ENST00000650293.1:c.396C>T
ENST00000288774.7:c.442C>T	ENSP00000288774.3:p.His148Tyr
ENST00000447513.6:c.442C>T	ENSP00000407922.2:p.His148Tyr
ENST00000502666.1:c.647C>T	ENSP00000461951.1:n.647C>T
ENST00000507596.5:c.442C>T	ENSP00000424291.1:p.His148Tyr
ENST00000508384.5:c.10C>T	ENSP00000464289.1:p.His4Tyr
ENST00000510434.1:c.442C>T	ENSP00000423051.1:p.His148Tyr
ENST00000515760.1:n.576C>T
NM_002617.3:c.442C>T	NP_002608.1:p.His148Tyr
NM_153818.1:c.442C>T	NP_722540.1:p.His148Tyr
XM_011541573.1:c.442C>T	XP_011539875.1:p.His148Tyr
XM_011541574.1:c.10C>T	XP_011539876.1:p.His4Tyr
XM_011541575.1:c.10C>T	XP_011539877.1:p.His4Tyr
XM_011541576.1:c.442C>T	XP_011539878.1:p.His148Tyr
XR_946666.1:n.562C>T
XM_011541576.2:c.442C>T	XP_011539878.1:p.His148Tyr
XR_946666.2:n.511C>T
NM_001374425.1:c.442C>T	NP_001361354.1:p.His148Tyr
NM_001374426.1:c.10C>T	NP_001361355.1:p.His4Tyr
NM_001374427.1:c.10C>T	NP_001361356.1:p.His4Tyr
NM_002617.4:c.442C>T MANE Select	NP_002608.1:p.His148Tyr
NM_153818.2:c.442C>T	NP_722540.1:p.His148Tyr
NR_164636.1:n.561C>T