Canonical Allele Identifier: CA337984085

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337937A>G (hg19) ; chr1:g.2406498A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406498A>G , CM000663.2:g.2406498A>G	GRCh38
NC_000001.10:g.2337937A>G , CM000663.1:g.2337937A>G	GRCh37
NC_000001.9:g.2327797A>G	NCBI36
NG_008342.1:g.11074T>C
NG_016128.1:g.19724A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.958T>C	ENSP00000288774.3:p.Trp320Arg
ENST00000447513.7:c.898T>C MANE Select	ENSP00000407922.2:p.Trp300Arg
ENST00000650293.1:c.852T>C
ENST00000288774.7:c.958T>C	ENSP00000288774.3:p.Trp320Arg
ENST00000447513.6:c.898T>C	ENSP00000407922.2:p.Trp300Arg
ENST00000507596.5:c.898T>C	ENSP00000424291.1:p.Trp300Arg
NM_002617.3:c.898T>C	NP_002608.1:p.Trp300Arg
NM_153818.1:c.958T>C	NP_722540.1:p.Trp320Arg
XM_011541573.1:c.955T>C	XP_011539875.1:p.Trp319Arg
XM_011541574.1:c.523T>C	XP_011539876.1:p.Trp175Arg
XM_011541575.1:c.523T>C	XP_011539877.1:p.Trp175Arg
XR_946666.1:n.1014T>C
XR_946666.2:n.963T>C
NM_001374425.1:c.955T>C	NP_001361354.1:p.Trp319Arg
NM_001374426.1:c.523T>C	NP_001361355.1:p.Trp175Arg
NM_001374427.1:c.466T>C	NP_001361356.1:p.Trp156Arg
NM_002617.4:c.898T>C MANE Select	NP_002608.1:p.Trp300Arg
NM_153818.2:c.958T>C	NP_722540.1:p.Trp320Arg
NR_164636.1:n.1013T>C