Canonical Allele Identifier: CA1725938480
Gene: PEX1 HGNC NCBI

Linked Data

dbSNP Id: rs1792085106

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92504545_92504546del , CM000669.2:g.92504545_92504546del GRCh38
NC_000007.13:g.92133859_92133860del , CM000669.1:g.92133859_92133860del GRCh37
NC_000007.12:g.91971795_91971796del NCBI36
NG_008341.1:g.28986_28987del
NG_008341.2:g.28986_28987del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2071+186_2071+187del MANE Select ENSP00000248633.4:n.2071+186_2071+187del
ENST00000248633.8:c.2071+186_2071+187del ENSP00000248633.4:n.2071+186_2071+187del
ENST00000428214.5:c.1901-1351_1901-1350del ENSP00000394413.1:n.1901-1351_1901-1350del
ENST00000438045.5:c.1105+186_1105+187del ENSP00000410438.1:n.1105+186_1105+187del
ENST00000484913.5:n.2110+186_2110+187del
ENST00000496420.5:n.1747+186_1747+187del
NM_000466.2:c.2071+186_2071+187del NP_000457.1:n.2071+186_2071+187del
NM_001282677.1:c.1901-1351_1901-1350del NP_001269606.1:n.1901-1351_1901-1350del
NM_001282678.1:c.1447+186_1447+187del NP_001269607.1:n.1447+186_1447+187del
XM_005250433.3:c.322+186_322+187del XP_005250490.1:n.322+186_322+187del
XR_242246.3:n.2167+186_2167+187del
XM_017012319.2:c.322+186_322+187del XP_016867808.1:n.322+186_322+187del
XR_001744808.2:n.1098+186_1098+187del
XR_242246.5:n.2118+186_2118+187del
NM_000466.3:c.2071+186_2071+187del MANE Select NP_000457.1:n.2071+186_2071+187del
NM_001282677.2:c.1901-1351_1901-1350del NP_001269606.1:n.1901-1351_1901-1350del
NM_001282678.2:c.1447+186_1447+187del NP_001269607.1:n.1447+186_1447+187del