Canonical Allele Identifier: CA1725938604
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92504662T= , CM000669.2:g.92504662T= GRCh38
NC_000007.13:g.92133976T= , CM000669.1:g.92133976T= GRCh37
NC_000007.12:g.91971912T= NCBI36
NG_008341.1:g.28870A=
NG_008341.2:g.28870A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2071+70A= MANE Select ENSP00000248633.4:n.2071+70A=
ENST00000248633.8:c.2071+70A= ENSP00000248633.4:n.2071+70A=
ENST00000428214.5:c.1901-1467A= ENSP00000394413.1:n.1901-1467A=
ENST00000438045.5:c.1105+70A= ENSP00000410438.1:n.1105+70A=
ENST00000484913.5:n.2110+70A=
ENST00000496420.5:n.1747+70A=
NM_000466.2:c.2071+70A= NP_000457.1:n.2071+70A=
NM_001282677.1:c.1901-1467A= NP_001269606.1:n.1901-1467A=
NM_001282678.1:c.1447+70A= NP_001269607.1:n.1447+70A=
XM_005250433.3:c.322+70A= XP_005250490.1:n.322+70A=
XR_242246.3:n.2167+70A=
XM_017012319.2:c.322+70A= XP_016867808.1:n.322+70A=
XR_001744808.2:n.1098+70A=
XR_242246.5:n.2118+70A=
NM_000466.3:c.2071+70A= MANE Select NP_000457.1:n.2071+70A=
NM_001282677.2:c.1901-1467A= NP_001269606.1:n.1901-1467A=
NM_001282678.2:c.1447+70A= NP_001269607.1:n.1447+70A=