Canonical Allele Identifier: CA1725933496
Gene: PEX1 HGNC NCBI

Linked Data

dbSNP Id: rs1791676964

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92496842_92496843insG , CM000669.2:g.92496842_92496843insG GRCh38
NC_000007.13:g.92126156_92126157insG , CM000669.1:g.92126156_92126157insG GRCh37
NC_000007.12:g.91964092_91964093insG NCBI36
NG_008341.1:g.36689_36690insC
NG_008341.2:g.36689_36690insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2719-66_2719-65insC MANE Select ENSP00000248633.4:n.2719-66_2719-65insC
ENST00000248633.8:c.2719-66_2719-65insC ENSP00000248633.4:n.2719-66_2719-65insC
ENST00000428214.5:c.2548-66_2548-65insC ENSP00000394413.1:n.2548-66_2548-65insC
ENST00000438045.5:c.1753-66_1753-65insC ENSP00000410438.1:n.1753-66_1753-65insC
ENST00000484913.5:n.2758-66_2758-65insC
ENST00000496420.5:n.2611-66_2611-65insC
NM_000466.2:c.2719-66_2719-65insC NP_000457.1:n.2719-66_2719-65insC
NM_001282677.1:c.2548-66_2548-65insC NP_001269606.1:n.2548-66_2548-65insC
NM_001282678.1:c.2095-66_2095-65insC NP_001269607.1:n.2095-66_2095-65insC
XM_005250433.3:c.970-66_970-65insC XP_005250490.1:n.970-66_970-65insC
XR_242246.3:n.2815-66_2815-65insC
XM_017012319.2:c.970-66_970-65insC XP_016867808.1:n.970-66_970-65insC
XR_001744808.2:n.1746-66_1746-65insC
XR_242246.5:n.2766-66_2766-65insC
NM_000466.3:c.2719-66_2719-65insC MANE Select NP_000457.1:n.2719-66_2719-65insC
NM_001282677.2:c.2548-66_2548-65insC NP_001269606.1:n.2548-66_2548-65insC
NM_001282678.2:c.2095-66_2095-65insC NP_001269607.1:n.2095-66_2095-65insC