Canonical Allele Identifier: CA1104476439
Gene: PEX1 HGNC NCBI

Linked Data

dbSNP Id: rs1792826656

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517166_92517167del , CM000669.2:g.92517166_92517167del GRCh38
NC_000007.13:g.92146480_92146481del , CM000669.1:g.92146480_92146481del GRCh37
NC_000007.12:g.91984416_91984417del NCBI36
NG_008341.1:g.16368_16369del
NG_008341.2:g.16368_16369del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1239+112_1239+113del MANE Select ENSP00000248633.4:n.1239+112_1239+113del
ENST00000248633.8:c.1239+112_1239+113del ENSP00000248633.4:n.1239+112_1239+113del
ENST00000422866.1:c.140+112_140+113del
ENST00000428214.5:c.1239+112_1239+113del ENSP00000394413.1:n.1239+112_1239+113del
ENST00000438045.5:c.274-3197_274-3196del ENSP00000410438.1:n.274-3197_274-3196del
ENST00000484913.5:n.1278+112_1278+113del
NM_000466.2:c.1239+112_1239+113del NP_000457.1:n.1239+112_1239+113del
NM_001282677.1:c.1239+112_1239+113del NP_001269606.1:n.1239+112_1239+113del
NM_001282678.1:c.615+112_615+113del NP_001269607.1:n.615+112_615+113del
XR_242246.3:n.1335+112_1335+113del
XM_017012319.2:c.-428+112_-428+113del XP_016867808.1:n.-428+112_-428+113del
XR_001744808.2:n.349+112_349+113del
XR_242246.5:n.1286+112_1286+113del
NM_000466.3:c.1239+112_1239+113del MANE Select NP_000457.1:n.1239+112_1239+113del
NM_001282677.2:c.1239+112_1239+113del NP_001269606.1:n.1239+112_1239+113del
NM_001282678.2:c.615+112_615+113del NP_001269607.1:n.615+112_615+113del