Canonical Allele Identifier: CA337984196

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337955A>G (hg19) ; chr1:g.2406516A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406516A>G , CM000663.2:g.2406516A>G	GRCh38
NC_000001.10:g.2337955A>G , CM000663.1:g.2337955A>G	GRCh37
NC_000001.9:g.2327815A>G	NCBI36
NG_008342.1:g.11056T>C
NG_016128.1:g.19742A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.940T>C	ENSP00000288774.3:p.Trp314Arg
ENST00000447513.7:c.880T>C MANE Select	ENSP00000407922.2:p.Trp294Arg
ENST00000650293.1:c.834T>C
ENST00000288774.7:c.940T>C	ENSP00000288774.3:p.Trp314Arg
ENST00000447513.6:c.880T>C	ENSP00000407922.2:p.Trp294Arg
ENST00000507596.5:c.880T>C	ENSP00000424291.1:p.Trp294Arg
NM_002617.3:c.880T>C	NP_002608.1:p.Trp294Arg
NM_153818.1:c.940T>C	NP_722540.1:p.Trp314Arg
XM_011541573.1:c.937T>C	XP_011539875.1:p.Trp313Arg
XM_011541574.1:c.505T>C	XP_011539876.1:p.Trp169Arg
XM_011541575.1:c.505T>C	XP_011539877.1:p.Trp169Arg
XR_946666.1:n.996T>C
XR_946666.2:n.945T>C
NM_001374425.1:c.937T>C	NP_001361354.1:p.Trp313Arg
NM_001374426.1:c.505T>C	NP_001361355.1:p.Trp169Arg
NM_001374427.1:c.448T>C	NP_001361356.1:p.Trp150Arg
NM_002617.4:c.880T>C MANE Select	NP_002608.1:p.Trp294Arg
NM_153818.2:c.940T>C	NP_722540.1:p.Trp314Arg
NR_164636.1:n.995T>C