Canonical Allele Identifier: CA1725931034

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494305A= , CM000669.2:g.92494305A= GRCh38
NC_000007.13:g.92123619A= , CM000669.1:g.92123619A= GRCh37
NC_000007.12:g.91961555A= NCBI36
NG_008341.1:g.39227T=
NG_008341.2:g.39227T=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3018T= (PEX1) MANE Select ENSP00000248633.4:p.Pro1006=
ENST00000248633.8:c.3018T= (PEX1) ENSP00000248633.4:p.Pro1006=
ENST00000428214.5:c.2847T= (PEX1) ENSP00000394413.1:p.Pro949=
ENST00000438045.5:c.2052T= (PEX1) ENSP00000410438.1:p.Pro684=
ENST00000484913.5:n.3057T= (PEX1)
ENST00000496420.5:n.2910T= (PEX1)
NM_000466.2:c.3018T= (PEX1) NP_000457.1:p.Pro1006=
NM_001282677.1:c.2847T= (PEX1) NP_001269606.1:p.Pro949=
NM_001282678.1:c.2394T= (PEX1) NP_001269607.1:p.Pro798=
XM_005250433.3:c.1269T= (PEX1) XP_005250490.1:p.Pro423=
XR_242246.3:n.3114T= (PEX1)
XM_017012319.2:c.1269T= (PEX1) XP_016867808.1:p.Pro423=
XR_001744808.2:n.2045T= (PEX1)
XR_001744843.2:n.5274A= (GATAD1)
XR_242246.5:n.3065T= (PEX1)
XR_927494.3:n.4125A= (GATAD1)
XR_927503.3:n.4056A= (GATAD1)
NM_000466.3:c.3018T= (PEX1) MANE Select NP_000457.1:p.Pro1006=
NM_001282677.2:c.2847T= (PEX1) NP_001269606.1:p.Pro949=
NM_001282678.2:c.2394T= (PEX1) NP_001269607.1:p.Pro798=