Canonical Allele Identifier: CA1149571912
Gene: PEX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408778G= , CM000663.2:g.2408778G= GRCh38
NC_000001.10:g.2340217G= , CM000663.1:g.2340217G= GRCh37
NC_000001.9:g.2330077G= NCBI36
NG_008342.1:g.8794C=

Transcript Alleles

HGVS Amino-acid change
ENST00000288774.8:c.274C= ENSP00000288774.3:p.Arg92=
ENST00000447513.7:c.274C= MANE Select ENSP00000407922.2:p.Arg92=
ENST00000650293.1:c.228C=
ENST00000288774.7:c.274C= ENSP00000288774.3:p.Arg92=
ENST00000447513.6:c.274C= ENSP00000407922.2:p.Arg92=
ENST00000502666.1:c.479C= ENSP00000461951.1:n.479C=
ENST00000507596.5:c.274C= ENSP00000424291.1:p.Arg92=
ENST00000508384.5:c.-159C= ENSP00000464289.1:n.-159C=
ENST00000510434.1:c.274C= ENSP00000423051.1:p.Arg92=
ENST00000514502.1:c.*291C= ENSP00000425924.1:n.*291C=
ENST00000515760.1:n.408C=
NM_002617.3:c.274C= NP_002608.1:p.Arg92=
NM_153818.1:c.274C= NP_722540.1:p.Arg92=
XM_011541573.1:c.274C= XP_011539875.1:p.Arg92=
XM_011541574.1:c.-159C= XP_011539876.1:n.-159C=
XM_011541575.1:c.-159C= XP_011539877.1:n.-159C=
XM_011541576.1:c.274C= XP_011539878.1:p.Arg92=
XR_946666.1:n.394C=
XM_011541576.2:c.274C= XP_011539878.1:p.Arg92=
XR_946666.2:n.343C=
NM_001374425.1:c.274C= NP_001361354.1:p.Arg92=
NM_001374426.1:c.-159C= NP_001361355.1:n.-159C=
NM_001374427.1:c.-159C= NP_001361356.1:n.-159C=
NM_002617.4:c.274C= MANE Select NP_002608.1:p.Arg92=
NM_153818.2:c.274C= NP_722540.1:p.Arg92=
NR_164636.1:n.393C=