Canonical Allele Identifier: CA1725948085
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517906T= , CM000669.2:g.92517906T= GRCh38
NC_000007.13:g.92147220T= , CM000669.1:g.92147220T= GRCh37
NC_000007.12:g.91985156T= NCBI36
NG_008341.1:g.15626A=
NG_008341.2:g.15626A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.609A= MANE Select ENSP00000248633.4:p.Gly203=
ENST00000248633.8:c.609A= ENSP00000248633.4:p.Gly203=
ENST00000428214.5:c.609A= ENSP00000394413.1:p.Gly203=
ENST00000438045.5:c.274-3939A= ENSP00000410438.1:n.274-3939A=
ENST00000484913.5:n.648A=
NM_000466.2:c.609A= NP_000457.1:p.Gly203=
NM_001282677.1:c.609A= NP_001269606.1:p.Gly203=
NM_001282678.1:c.-16A= NP_001269607.1:n.-16A=
XR_242246.3:n.705A=
XR_242246.5:n.656A=
NM_000466.3:c.609A= MANE Select NP_000457.1:p.Gly203=
NM_001282677.2:c.609A= NP_001269606.1:p.Gly203=
NM_001282678.2:c.-16A= NP_001269607.1:n.-16A=