Canonical Allele Identifier: CA337984197

Gene: PEX10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.940T>G	ENSP00000288774.3:p.Trp314Gly
ENST00000447513.7:c.880T>G MANE Select	ENSP00000407922.2:p.Trp294Gly
ENST00000650293.1:c.834T>G
ENST00000288774.7:c.940T>G	ENSP00000288774.3:p.Trp314Gly
ENST00000447513.6:c.880T>G	ENSP00000407922.2:p.Trp294Gly
ENST00000507596.5:c.880T>G	ENSP00000424291.1:p.Trp294Gly
NM_002617.3:c.880T>G	NP_002608.1:p.Trp294Gly
NM_153818.1:c.940T>G	NP_722540.1:p.Trp314Gly
XM_011541573.1:c.937T>G	XP_011539875.1:p.Trp313Gly
XM_011541574.1:c.505T>G	XP_011539876.1:p.Trp169Gly
XM_011541575.1:c.505T>G	XP_011539877.1:p.Trp169Gly
XR_946666.1:n.996T>G
XR_946666.2:n.945T>G
NM_001374425.1:c.937T>G	NP_001361354.1:p.Trp313Gly
NM_001374426.1:c.505T>G	NP_001361355.1:p.Trp169Gly
NM_001374427.1:c.448T>G	NP_001361356.1:p.Trp150Gly
NM_002617.4:c.880T>G MANE Select	NP_002608.1:p.Trp294Gly
NM_153818.2:c.940T>G	NP_722540.1:p.Trp314Gly
NR_164636.1:n.995T>G