Canonical Allele Identifier: CA1149570804
Gene: PEX10 HGNC NCBI

Linked Data

dbSNP Id: rs1557908370
gnomAD v4: 1-2406454-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2406454C>A , CM000663.2:g.2406454C>A GRCh38
NC_000001.10:g.2337893C>A , CM000663.1:g.2337893C>A GRCh37
NC_000001.9:g.2327753C>A NCBI36
NG_008342.1:g.11118G>T
NG_016128.1:g.19680C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000288774.8:c.972+30G>T ENSP00000288774.3:n.972+30G>T
ENST00000447513.7:c.912+30G>T MANE Select ENSP00000407922.2:n.912+30G>T
ENST00000650293.1:c.866+30G>T
ENST00000288774.7:c.972+30G>T ENSP00000288774.3:n.972+30G>T
ENST00000447513.6:c.912+30G>T ENSP00000407922.2:n.912+30G>T
ENST00000507596.5:c.912+30G>T ENSP00000424291.1:n.912+30G>T
NM_002617.3:c.912+30G>T NP_002608.1:n.912+30G>T
NM_153818.1:c.972+30G>T NP_722540.1:n.972+30G>T
XM_011541573.1:c.969+30G>T XP_011539875.1:n.969+30G>T
XM_011541574.1:c.537+30G>T XP_011539876.1:n.537+30G>T
XM_011541575.1:c.537+30G>T XP_011539877.1:n.537+30G>T
XR_946666.1:n.1028+30G>T
XR_946666.2:n.977+30G>T
NM_001374425.1:c.969+30G>T NP_001361354.1:n.969+30G>T
NM_001374426.1:c.537+30G>T NP_001361355.1:n.537+30G>T
NM_001374427.1:c.480+30G>T NP_001361356.1:n.480+30G>T
NM_002617.4:c.912+30G>T MANE Select NP_002608.1:n.912+30G>T
NM_153818.2:c.972+30G>T NP_722540.1:n.972+30G>T
NR_164636.1:n.1027+30G>T