Canonical Allele Identifier: CA2776945569

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491550_92491553del , CM000669.2:g.92491550_92491553del GRCh38
NC_000007.13:g.92120864_92120867del , CM000669.1:g.92120864_92120867del GRCh37
NC_000007.12:g.91958800_91958803del NCBI36
NG_008341.1:g.41979_41982del
NG_008341.2:g.41979_41982del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3208-51_3208-48del (PEX1) MANE Select ENSP00000248633.4:n.3208-51_3208-48del
ENST00000248633.8:c.3208-51_3208-48del (PEX1) ENSP00000248633.4:n.3208-51_3208-48del
ENST00000428214.5:c.3037-51_3037-48del (PEX1) ENSP00000394413.1:n.3037-51_3037-48del
ENST00000438045.5:c.2242-51_2242-48del (PEX1) ENSP00000410438.1:n.2242-51_2242-48del
ENST00000484913.5:n.3247-51_3247-48del (PEX1)
ENST00000496420.5:n.4263-51_4263-48del (PEX1)
NM_000466.2:c.3208-51_3208-48del (PEX1) NP_000457.1:n.3208-51_3208-48del
NM_001282677.1:c.3037-51_3037-48del (PEX1) NP_001269606.1:n.3037-51_3037-48del
NM_001282678.1:c.2584-51_2584-48del (PEX1) NP_001269607.1:n.2584-51_2584-48del
XM_005250433.3:c.1459-51_1459-48del (PEX1) XP_005250490.1:n.1459-51_1459-48del
XR_242246.3:n.3304-51_3304-48del (PEX1)
XM_017012319.2:c.1459-51_1459-48del (PEX1) XP_016867808.1:n.1459-51_1459-48del
XR_001744808.2:n.2235-51_2235-48del (PEX1)
XR_001744842.2:n.2588_2591del (GATAD1)
XR_001744843.2:n.2519_2522del (GATAD1)
XR_002956472.1:n.2645_2648del (GATAD1)
XR_002956473.1:n.2676_2679del (GATAD1)
XR_002956474.1:n.2593_2596del (GATAD1)
XR_242246.5:n.3255-51_3255-48del (PEX1)
XR_927494.3:n.1370_1373del (GATAD1)
XR_927500.3:n.1367_1370del (GATAD1)
XR_927503.3:n.1301_1304del (GATAD1)
NM_000466.3:c.3208-51_3208-48del (PEX1) MANE Select NP_000457.1:n.3208-51_3208-48del
NM_001282677.2:c.3037-51_3037-48del (PEX1) NP_001269606.1:n.3037-51_3037-48del
NM_001282678.2:c.2584-51_2584-48del (PEX1) NP_001269607.1:n.2584-51_2584-48del