Canonical Allele Identifier: CA1725947681
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517670G= , CM000669.2:g.92517670G= GRCh38
NC_000007.13:g.92146984G= , CM000669.1:g.92146984G= GRCh37
NC_000007.12:g.91984920G= NCBI36
NG_008341.1:g.15862C=
NG_008341.2:g.15862C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.845C= MANE Select ENSP00000248633.4:p.Pro282=
ENST00000248633.8:c.845C= ENSP00000248633.4:p.Pro282=
ENST00000428214.5:c.845C= ENSP00000394413.1:p.Pro282=
ENST00000438045.5:c.274-3703C= ENSP00000410438.1:n.274-3703C=
ENST00000484913.5:n.884C=
NM_000466.2:c.845C= NP_000457.1:p.Pro282=
NM_001282677.1:c.845C= NP_001269606.1:p.Pro282=
NM_001282678.1:c.221C= NP_001269607.1:p.Pro74=
XR_242246.3:n.941C=
XR_242246.5:n.892C=
NM_000466.3:c.845C= MANE Select NP_000457.1:p.Pro282=
NM_001282677.2:c.845C= NP_001269606.1:p.Pro282=
NM_001282678.2:c.221C= NP_001269607.1:p.Pro74=