Canonical Allele Identifier: CA2776945672
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92496894_92496896del , CM000669.2:g.92496894_92496896del GRCh38
NC_000007.13:g.92126208_92126210del , CM000669.1:g.92126208_92126210del GRCh37
NC_000007.12:g.91964144_91964146del NCBI36
NG_008341.1:g.36637_36639del
NG_008341.2:g.36637_36639del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2719-118_2719-116del MANE Select ENSP00000248633.4:n.2719-118_2719-116del
ENST00000248633.8:c.2719-118_2719-116del ENSP00000248633.4:n.2719-118_2719-116del
ENST00000428214.5:c.2548-118_2548-116del ENSP00000394413.1:n.2548-118_2548-116del
ENST00000438045.5:c.1753-118_1753-116del ENSP00000410438.1:n.1753-118_1753-116del
ENST00000484913.5:n.2758-118_2758-116del
ENST00000496420.5:n.2611-118_2611-116del
NM_000466.2:c.2719-118_2719-116del NP_000457.1:n.2719-118_2719-116del
NM_001282677.1:c.2548-118_2548-116del NP_001269606.1:n.2548-118_2548-116del
NM_001282678.1:c.2095-118_2095-116del NP_001269607.1:n.2095-118_2095-116del
XM_005250433.3:c.970-118_970-116del XP_005250490.1:n.970-118_970-116del
XR_242246.3:n.2815-118_2815-116del
XM_017012319.2:c.970-118_970-116del XP_016867808.1:n.970-118_970-116del
XR_001744808.2:n.1746-118_1746-116del
XR_242246.5:n.2766-118_2766-116del
NM_000466.3:c.2719-118_2719-116del MANE Select NP_000457.1:n.2719-118_2719-116del
NM_001282677.2:c.2548-118_2548-116del NP_001269606.1:n.2548-118_2548-116del
NM_001282678.2:c.2095-118_2095-116del NP_001269607.1:n.2095-118_2095-116del