Canonical Allele Identifier: CA2776947277
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92511071_92511078del , CM000669.2:g.92511071_92511078del GRCh38
NC_000007.13:g.92140385_92140392del , CM000669.1:g.92140385_92140392del GRCh37
NC_000007.12:g.91978321_91978328del NCBI36
NG_008341.1:g.22455_22462del
NG_008341.2:g.22455_22462del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1484-30_1484-23del MANE Select ENSP00000248633.4:n.1484-30_1484-23del
ENST00000248633.8:c.1484-30_1484-23del ENSP00000248633.4:n.1484-30_1484-23del
ENST00000422866.1:c.385-30_385-23del
ENST00000428214.5:c.1484-30_1484-23del ENSP00000394413.1:n.1484-30_1484-23del
ENST00000438045.5:c.518-30_518-23del ENSP00000410438.1:n.518-30_518-23del
ENST00000476923.1:n.245-30_245-23del
ENST00000484913.5:n.1523-30_1523-23del
NM_000466.2:c.1484-30_1484-23del NP_000457.1:n.1484-30_1484-23del
NM_001282677.1:c.1484-30_1484-23del NP_001269606.1:n.1484-30_1484-23del
NM_001282678.1:c.860-30_860-23del NP_001269607.1:n.860-30_860-23del
XM_005250433.3:c.-183-30_-183-23del XP_005250490.1:n.-183-30_-183-23del
XR_242246.3:n.1580-30_1580-23del
XM_017012319.2:c.-183-30_-183-23del XP_016867808.1:n.-183-30_-183-23del
XR_001744808.2:n.594-30_594-23del
XR_242246.5:n.1531-30_1531-23del
NM_000466.3:c.1484-30_1484-23del MANE Select NP_000457.1:n.1484-30_1484-23del
NM_001282677.2:c.1484-30_1484-23del NP_001269606.1:n.1484-30_1484-23del
NM_001282678.2:c.860-30_860-23del NP_001269607.1:n.860-30_860-23del