Canonical Allele Identifier: CA1725941884
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92506924A= , CM000669.2:g.92506924A= GRCh38
NC_000007.13:g.92136238A= , CM000669.1:g.92136238A= GRCh37
NC_000007.12:g.91974174A= NCBI36
NG_008341.1:g.26608T=
NG_008341.2:g.26608T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1803+70T= MANE Select ENSP00000248633.4:n.1803+70T=
ENST00000248633.8:c.1803+70T= ENSP00000248633.4:n.1803+70T=
ENST00000422866.1:c.621+70T=
ENST00000428214.5:c.1803+70T= ENSP00000394413.1:n.1803+70T=
ENST00000438045.5:c.837+70T= ENSP00000410438.1:n.837+70T=
ENST00000484913.5:n.1842+70T=
ENST00000496420.5:n.900T=
NM_000466.2:c.1803+70T= NP_000457.1:n.1803+70T=
NM_001282677.1:c.1803+70T= NP_001269606.1:n.1803+70T=
NM_001282678.1:c.1179+70T= NP_001269607.1:n.1179+70T=
XM_005250433.3:c.54+70T= XP_005250490.1:n.54+70T=
XR_242246.3:n.1899+70T=
XM_017012319.2:c.54+70T= XP_016867808.1:n.54+70T=
XR_001744808.2:n.830+70T=
XR_242246.5:n.1850+70T=
NM_000466.3:c.1803+70T= MANE Select NP_000457.1:n.1803+70T=
NM_001282677.2:c.1803+70T= NP_001269606.1:n.1803+70T=
NM_001282678.2:c.1179+70T= NP_001269607.1:n.1179+70T=