Canonical Allele Identifier: CA1725947520
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517568G= , CM000669.2:g.92517568G= GRCh38
NC_000007.13:g.92146882G= , CM000669.1:g.92146882G= GRCh37
NC_000007.12:g.91984818G= NCBI36
NG_008341.1:g.15964C=
NG_008341.2:g.15964C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.947C= MANE Select ENSP00000248633.4:p.Pro316=
ENST00000248633.8:c.947C= ENSP00000248633.4:p.Pro316=
ENST00000428214.5:c.947C= ENSP00000394413.1:p.Pro316=
ENST00000438045.5:c.274-3601C= ENSP00000410438.1:n.274-3601C=
ENST00000484913.5:n.986C=
NM_000466.2:c.947C= NP_000457.1:p.Pro316=
NM_001282677.1:c.947C= NP_001269606.1:p.Pro316=
NM_001282678.1:c.323C= NP_001269607.1:p.Pro108=
XR_242246.3:n.1043C=
XM_017012319.2:c.-720C= XP_016867808.1:n.-720C=
XR_001744808.2:n.57C=
XR_242246.5:n.994C=
NM_000466.3:c.947C= MANE Select NP_000457.1:p.Pro316=
NM_001282677.2:c.947C= NP_001269606.1:p.Pro316=
NM_001282678.2:c.323C= NP_001269607.1:p.Pro108=