Canonical Allele Identifier: CA1725935195
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92499811T= , CM000669.2:g.92499811T= GRCh38
NC_000007.13:g.92129125T= , CM000669.1:g.92129125T= GRCh37
NC_000007.12:g.91967061T= NCBI36
NG_008341.1:g.33721A=
NG_008341.2:g.33721A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2611A= MANE Select ENSP00000248633.4:p.Ile871=
ENST00000248633.8:c.2611A= ENSP00000248633.4:p.Ile871=
ENST00000428214.5:c.2440A= ENSP00000394413.1:p.Ile814=
ENST00000438045.5:c.1645A= ENSP00000410438.1:p.Ile549=
ENST00000484913.5:n.2650A=
ENST00000496420.5:n.2503A=
NM_000466.2:c.2611A= NP_000457.1:p.Ile871=
NM_001282677.1:c.2440A= NP_001269606.1:p.Ile814=
NM_001282678.1:c.1987A= NP_001269607.1:p.Ile663=
XM_005250433.3:c.862A= XP_005250490.1:p.Ile288=
XR_242246.3:n.2707A=
XM_017012319.2:c.862A= XP_016867808.1:p.Ile288=
XR_001744808.2:n.1638A=
XR_242246.5:n.2658A=
NM_000466.3:c.2611A= MANE Select NP_000457.1:p.Ile871=
NM_001282677.2:c.2440A= NP_001269606.1:p.Ile814=
NM_001282678.2:c.1987A= NP_001269607.1:p.Ile663=