Canonical Allele Identifier: CA415775809

Gene: PEX10

Linked Data

• ClinVar Variation Id: 1162053
• ClinVar RCV Id: RCV001506823
• dbSNP Id: rs767442631
• gnomAD v2: 1-2340002-C-A
• gnomAD v3: 1-2408563-C-A
• gnomAD v4: 1-2408563-C-A
• MyVariant Identifiers: chr1:g.2340002C>A (hg19) ; chr1:g.2408563C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408563C>A , CM000663.2:g.2408563C>A	GRCh38
NC_000001.10:g.2340002C>A , CM000663.1:g.2340002C>A	GRCh37
NC_000001.9:g.2329862C>A	NCBI36
NG_008342.1:g.9009G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.489G>T	ENSP00000288774.3:p.Ala163=
ENST00000447513.7:c.489G>T MANE Select	ENSP00000407922.2:p.Ala163=
ENST00000650293.1:c.443G>T
ENST00000288774.7:c.489G>T	ENSP00000288774.3:p.Ala163=
ENST00000447513.6:c.489G>T	ENSP00000407922.2:p.Ala163=
ENST00000507596.5:c.489G>T	ENSP00000424291.1:p.Ala163=
ENST00000508384.5:c.57G>T	ENSP00000464289.1:p.Ala19=
ENST00000510434.1:c.489G>T	ENSP00000423051.1:p.Ala163=
NM_002617.3:c.489G>T	NP_002608.1:p.Ala163=
NM_153818.1:c.489G>T	NP_722540.1:p.Ala163=
XM_011541573.1:c.489G>T	XP_011539875.1:p.Ala163=
XM_011541574.1:c.57G>T	XP_011539876.1:p.Ala19=
XM_011541575.1:c.57G>T	XP_011539877.1:p.Ala19=
XM_011541576.1:c.489G>T	XP_011539878.1:p.Ala163=
XR_946666.1:n.609G>T
XM_011541576.2:c.489G>T	XP_011539878.1:p.Ala163=
XR_946666.2:n.558G>T
NM_001374425.1:c.489G>T	NP_001361354.1:p.Ala163=
NM_001374426.1:c.57G>T	NP_001361355.1:p.Ala19=
NM_001374427.1:c.57G>T	NP_001361356.1:p.Ala19=
NM_002617.4:c.489G>T MANE Select	NP_002608.1:p.Ala163=
NM_153818.2:c.489G>T	NP_722540.1:p.Ala163=
NR_164636.1:n.608G>T