Canonical Allele Identifier: CA4341536
Community Standard Title: NM_000466.3(PEX1):c.803C>G (p.Thr268Ser)
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517712G>C , CM000669.2:g.92517712G>C GRCh38
NC_000007.13:g.92147026G>C , CM000669.1:g.92147026G>C GRCh37
NC_000007.12:g.91984962G>C NCBI36
NG_008341.1:g.15820C>G
NG_008341.2:g.15820C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000466.3:c.803C>G MANE Select NP_000457.1:p.Thr268Ser
ENST00000248633.9:c.803C>G MANE Select ENSP00000248633.4:p.Thr268Ser
NM_000466.2:c.803C>G NP_000457.1:p.Thr268Ser
NM_001282677.1:c.803C>G NP_001269606.1:p.Thr268Ser
NM_001282677.2:c.803C>G NP_001269606.1:p.Thr268Ser
NM_001282678.1:c.179C>G NP_001269607.1:p.Thr60Ser
NM_001282678.2:c.179C>G NP_001269607.1:p.Thr60Ser
ENST00000248633.8:c.803C>G ENSP00000248633.4:p.Thr268Ser
ENST00000428214.5:c.803C>G ENSP00000394413.1:p.Thr268Ser
ENST00000438045.5:c.274-3745C>G ENSP00000410438.1:n.274-3745C>G
ENST00000484913.5:n.842C>G
XR_242246.3:n.899C>G
XR_242246.5:n.850C>G