Canonical Allele Identifier: CA1725948711
Gene: PEX1 HGNC NCBI

Linked Data

dbSNP Id: rs1792901364

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518345del , CM000669.2:g.92518345del GRCh38
NC_000007.13:g.92147659del , CM000669.1:g.92147659del GRCh37
NC_000007.12:g.91985595del NCBI36
NG_008341.1:g.15192del
NG_008341.2:g.15192del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.358-85del MANE Select ENSP00000248633.4:n.358-85del
ENST00000248633.8:c.358-85del ENSP00000248633.4:n.358-85del
ENST00000428214.5:c.358-85del ENSP00000394413.1:n.358-85del
ENST00000438045.5:c.273+3762del ENSP00000410438.1:n.273+3762del
ENST00000484913.5:n.397-85del
NM_000466.2:c.358-85del NP_000457.1:n.358-85del
NM_001282677.1:c.358-85del NP_001269606.1:n.358-85del
NM_001282678.1:c.-267-85del NP_001269607.1:n.-267-85del
XR_242246.3:n.454-85del
XR_242246.5:n.405-85del
NM_000466.3:c.358-85del MANE Select NP_000457.1:n.358-85del
NM_001282677.2:c.358-85del NP_001269606.1:n.358-85del
NM_001282678.2:c.-267-85del NP_001269607.1:n.-267-85del