Canonical Allele Identifier: CA2776945562

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491530_92491548del , CM000669.2:g.92491530_92491548del GRCh38
NC_000007.13:g.92120844_92120862del , CM000669.1:g.92120844_92120862del GRCh37
NC_000007.12:g.91958780_91958798del NCBI36
NG_008341.1:g.41986_42004del
NG_008341.2:g.41986_42004del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3208-44_3208-26del (PEX1) MANE Select ENSP00000248633.4:n.3208-44_3208-26del
ENST00000248633.8:c.3208-44_3208-26del (PEX1) ENSP00000248633.4:n.3208-44_3208-26del
ENST00000428214.5:c.3037-44_3037-26del (PEX1) ENSP00000394413.1:n.3037-44_3037-26del
ENST00000438045.5:c.2242-44_2242-26del (PEX1) ENSP00000410438.1:n.2242-44_2242-26del
ENST00000484913.5:n.3247-44_3247-26del (PEX1)
ENST00000496420.5:n.4263-44_4263-26del (PEX1)
NM_000466.2:c.3208-44_3208-26del (PEX1) NP_000457.1:n.3208-44_3208-26del
NM_001282677.1:c.3037-44_3037-26del (PEX1) NP_001269606.1:n.3037-44_3037-26del
NM_001282678.1:c.2584-44_2584-26del (PEX1) NP_001269607.1:n.2584-44_2584-26del
XM_005250433.3:c.1459-44_1459-26del (PEX1) XP_005250490.1:n.1459-44_1459-26del
XR_242246.3:n.3304-44_3304-26del (PEX1)
XM_017012319.2:c.1459-44_1459-26del (PEX1) XP_016867808.1:n.1459-44_1459-26del
XR_001744808.2:n.2235-44_2235-26del (PEX1)
XR_001744842.2:n.2568_2586del (GATAD1)
XR_001744843.2:n.2499_2517del (GATAD1)
XR_002956472.1:n.2625_2643del (GATAD1)
XR_002956473.1:n.2656_2674del (GATAD1)
XR_002956474.1:n.2573_2591del (GATAD1)
XR_242246.5:n.3255-44_3255-26del (PEX1)
XR_927494.3:n.1350_1368del (GATAD1)
XR_927500.3:n.1347_1365del (GATAD1)
XR_927503.3:n.1281_1299del (GATAD1)
NM_000466.3:c.3208-44_3208-26del (PEX1) MANE Select NP_000457.1:n.3208-44_3208-26del
NM_001282677.2:c.3037-44_3037-26del (PEX1) NP_001269606.1:n.3037-44_3037-26del
NM_001282678.2:c.2584-44_2584-26del (PEX1) NP_001269607.1:n.2584-44_2584-26del