Canonical Allele Identifier: CA368183095
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92504771G>A , CM000669.2:g.92504771G>A GRCh38
NC_000007.13:g.92134085G>A , CM000669.1:g.92134085G>A GRCh37
NC_000007.12:g.91972021G>A NCBI36
NG_008341.1:g.28761C>T
NG_008341.2:g.28761C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2032C>T MANE Select ENSP00000248633.4:p.His678Tyr
ENST00000248633.8:c.2032C>T ENSP00000248633.4:p.His678Tyr
ENST00000428214.5:n.1900+1477C>T ENSP00000394413.1:p.=
ENST00000438045.5:c.1066C>T ENSP00000410438.1:p.His356Tyr
ENST00000484913.5:n.2071C>T
ENST00000496420.5:n.1708C>T
NM_000466.2:c.2032C>T NP_000457.1:p.His678Tyr
NM_001282677.1:c.1900+1477C>T NP_001269606.1:p.=
NM_001282678.1:c.1408C>T NP_001269607.1:p.His470Tyr
XM_005250433.3:c.283C>T XP_005250490.1:p.His95Tyr
XR_242246.3:n.2128C>T
XM_017012319.2:c.283C>T XP_016867808.1:p.His95Tyr
XR_001744808.2:n.1059C>T
XR_242246.5:n.2079C>T
NM_000466.3:c.2032C>T MANE Select NP_000457.1:p.His678Tyr
NM_001282677.2:c.1900+1477C>T NP_001269606.1:p.=
NM_001282678.2:c.1408C>T NP_001269607.1:p.His470Tyr