Canonical Allele Identifier: CA16041152
Gene: PEX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 371721
dbSNP Id: rs1057517485

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92499736G>A , CM000669.2:g.92499736G>A GRCh38
NC_000007.13:g.92129050G>A , CM000669.1:g.92129050G>A GRCh37
NC_000007.12:g.91966986G>A NCBI36
NG_008341.1:g.33796C>T
NG_008341.2:g.33796C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2686C>T MANE Select ENSP00000248633.4:p.Arg896Ter
ENST00000248633.8:c.2686C>T ENSP00000248633.4:p.Arg896Ter
ENST00000428214.5:n.2515C>T ENSP00000394413.1:p.Arg839Ter
ENST00000438045.5:c.1720C>T ENSP00000410438.1:p.Arg574Ter
ENST00000484913.5:n.2725C>T
ENST00000496420.5:n.2578C>T
NM_000466.2:c.2686C>T NP_000457.1:p.Arg896Ter
NM_001282677.1:c.2515C>T NP_001269606.1:p.Arg839Ter
NM_001282678.1:c.2062C>T NP_001269607.1:p.Arg688Ter
XM_005250433.3:c.937C>T XP_005250490.1:p.Arg313Ter
XR_242246.3:n.2782C>T
XM_017012319.2:c.937C>T XP_016867808.1:p.Arg313Ter
XR_001744808.2:n.1713C>T
XR_242246.5:n.2733C>T
NM_000466.3:c.2686C>T MANE Select NP_000457.1:p.Arg896Ter
NM_001282677.2:c.2515C>T NP_001269606.1:p.Arg839Ter
NM_001282678.2:c.2062C>T NP_001269607.1:p.Arg688Ter