Canonical Allele Identifier: CA456484175
Community Standard Title: NM_000466.3(PEX1):c.96G>A (p.Pro32=)
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92528340C>T , CM000669.2:g.92528340C>T GRCh38
NC_000007.13:g.92157654C>T , CM000669.1:g.92157654C>T GRCh37
NC_000007.12:g.91995590C>T NCBI36
NG_008341.1:g.5192G>A
NG_008341.2:g.5192G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000466.3:c.96G>A MANE Select NP_000457.1:p.Pro32=
ENST00000248633.9:c.96G>A MANE Select ENSP00000248633.4:p.Pro32=
NM_000466.2:c.96G>A NP_000457.1:p.Pro32=
NM_001282677.1:c.96G>A NP_001269606.1:p.Pro32=
NM_001282677.2:c.96G>A NP_001269606.1:p.Pro32=
NM_001282678.1:c.-564G>A NP_001269607.1:n.-564G>A
NM_001282678.2:c.-564G>A NP_001269607.1:n.-564G>A
ENST00000248633.8:c.96G>A ENSP00000248633.4:p.Pro32=
ENST00000428214.5:c.96G>A ENSP00000394413.1:p.Pro32=
ENST00000438045.5:c.96G>A ENSP00000410438.1:p.Pro32=
ENST00000484913.5:n.100G>A
XR_242246.3:n.192G>A
XR_242246.5:n.143G>A