Canonical Allele Identifier: CA337984096

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337939G>C (hg19) ; chr1:g.2406500G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406500G>C , CM000663.2:g.2406500G>C	GRCh38
NC_000001.10:g.2337939G>C , CM000663.1:g.2337939G>C	GRCh37
NC_000001.9:g.2327799G>C	NCBI36
NG_008342.1:g.11072C>G
NG_016128.1:g.19726G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.956C>G	ENSP00000288774.3:p.Ala319Gly
ENST00000447513.7:c.896C>G MANE Select	ENSP00000407922.2:p.Ala299Gly
ENST00000650293.1:c.850C>G
ENST00000288774.7:c.956C>G	ENSP00000288774.3:p.Ala319Gly
ENST00000447513.6:c.896C>G	ENSP00000407922.2:p.Ala299Gly
ENST00000507596.5:c.896C>G	ENSP00000424291.1:p.Ala299Gly
NM_002617.3:c.896C>G	NP_002608.1:p.Ala299Gly
NM_153818.1:c.956C>G	NP_722540.1:p.Ala319Gly
XM_011541573.1:c.953C>G	XP_011539875.1:p.Ala318Gly
XM_011541574.1:c.521C>G	XP_011539876.1:p.Ala174Gly
XM_011541575.1:c.521C>G	XP_011539877.1:p.Ala174Gly
XR_946666.1:n.1012C>G
XR_946666.2:n.961C>G
NM_001374425.1:c.953C>G	NP_001361354.1:p.Ala318Gly
NM_001374426.1:c.521C>G	NP_001361355.1:p.Ala174Gly
NM_001374427.1:c.464C>G	NP_001361356.1:p.Ala155Gly
NM_002617.4:c.896C>G MANE Select	NP_002608.1:p.Ala299Gly
NM_153818.2:c.956C>G	NP_722540.1:p.Ala319Gly
NR_164636.1:n.1011C>G