Canonical Allele Identifier: CA337984205

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337958A>C (hg19) ; chr1:g.2406519A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406519A>C , CM000663.2:g.2406519A>C	GRCh38
NC_000001.10:g.2337958A>C , CM000663.1:g.2337958A>C	GRCh37
NC_000001.9:g.2327818A>C	NCBI36
NG_008342.1:g.11053T>G
NG_016128.1:g.19745A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.937T>G	ENSP00000288774.3:p.Cys313Gly
ENST00000447513.7:c.877T>G MANE Select	ENSP00000407922.2:p.Cys293Gly
ENST00000650293.1:c.831T>G
ENST00000288774.7:c.937T>G	ENSP00000288774.3:p.Cys313Gly
ENST00000447513.6:c.877T>G	ENSP00000407922.2:p.Cys293Gly
ENST00000507596.5:c.877T>G	ENSP00000424291.1:p.Cys293Gly
ENST00000510434.1:c.*243T>G	ENSP00000423051.1:n.*243T>G
NM_002617.3:c.877T>G	NP_002608.1:p.Cys293Gly
NM_153818.1:c.937T>G	NP_722540.1:p.Cys313Gly
XM_011541573.1:c.934T>G	XP_011539875.1:p.Cys312Gly
XM_011541574.1:c.502T>G	XP_011539876.1:p.Cys168Gly
XM_011541575.1:c.502T>G	XP_011539877.1:p.Cys168Gly
XR_946666.1:n.993T>G
XR_946666.2:n.942T>G
NM_001374425.1:c.934T>G	NP_001361354.1:p.Cys312Gly
NM_001374426.1:c.502T>G	NP_001361355.1:p.Cys168Gly
NM_001374427.1:c.445T>G	NP_001361356.1:p.Cys149Gly
NM_002617.4:c.877T>G MANE Select	NP_002608.1:p.Cys293Gly
NM_153818.2:c.937T>G	NP_722540.1:p.Cys313Gly
NR_164636.1:n.992T>G