Canonical Allele Identifier: CA733529040

Gene: PEX10

Linked Data

• dbSNP Id: rs1394876303
• gnomAD v4: 1-2406425-G-T
• MyVariant Identifiers: chr1:g.2337864G>T (hg19) ; chr1:g.2406425G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406425G>T , CM000663.2:g.2406425G>T	GRCh38
NC_000001.10:g.2337864G>T , CM000663.1:g.2337864G>T	GRCh37
NC_000001.9:g.2327724G>T	NCBI36
NG_008342.1:g.11147C>A
NG_016128.1:g.19651G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.972+59C>A	ENSP00000288774.3:n.972+59C>A
ENST00000447513.7:c.912+59C>A MANE Select	ENSP00000407922.2:n.912+59C>A
ENST00000650293.1:c.866+59C>A
ENST00000288774.7:c.972+59C>A	ENSP00000288774.3:n.972+59C>A
ENST00000447513.6:c.912+59C>A	ENSP00000407922.2:n.912+59C>A
ENST00000507596.5:c.912+59C>A	ENSP00000424291.1:n.912+59C>A
NM_002617.3:c.912+59C>A	NP_002608.1:n.912+59C>A
NM_153818.1:c.972+59C>A	NP_722540.1:n.972+59C>A
XM_011541573.1:c.969+59C>A	XP_011539875.1:n.969+59C>A
XM_011541574.1:c.537+59C>A	XP_011539876.1:n.537+59C>A
XM_011541575.1:c.537+59C>A	XP_011539877.1:n.537+59C>A
XR_946666.1:n.1028+59C>A
XR_946666.2:n.977+59C>A
NM_001374425.1:c.969+59C>A	NP_001361354.1:n.969+59C>A
NM_001374426.1:c.537+59C>A	NP_001361355.1:n.537+59C>A
NM_001374427.1:c.480+59C>A	NP_001361356.1:n.480+59C>A
NM_002617.4:c.912+59C>A MANE Select	NP_002608.1:n.912+59C>A
NM_153818.2:c.972+59C>A	NP_722540.1:n.972+59C>A
NR_164636.1:n.1027+59C>A