Canonical Allele Identifier: CA2776945579

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491564_92491568del , CM000669.2:g.92491564_92491568del GRCh38
NC_000007.13:g.92120878_92120882del , CM000669.1:g.92120878_92120882del GRCh37
NC_000007.12:g.91958814_91958818del NCBI36
NG_008341.1:g.41965_41969del
NG_008341.2:g.41965_41969del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3208-65_3208-61del (PEX1) MANE Select ENSP00000248633.4:n.3208-65_3208-61del
ENST00000248633.8:c.3208-65_3208-61del (PEX1) ENSP00000248633.4:n.3208-65_3208-61del
ENST00000428214.5:c.3037-65_3037-61del (PEX1) ENSP00000394413.1:n.3037-65_3037-61del
ENST00000438045.5:c.2242-65_2242-61del (PEX1) ENSP00000410438.1:n.2242-65_2242-61del
ENST00000484913.5:n.3247-65_3247-61del (PEX1)
ENST00000496420.5:n.4263-65_4263-61del (PEX1)
NM_000466.2:c.3208-65_3208-61del (PEX1) NP_000457.1:n.3208-65_3208-61del
NM_001282677.1:c.3037-65_3037-61del (PEX1) NP_001269606.1:n.3037-65_3037-61del
NM_001282678.1:c.2584-65_2584-61del (PEX1) NP_001269607.1:n.2584-65_2584-61del
XM_005250433.3:c.1459-65_1459-61del (PEX1) XP_005250490.1:n.1459-65_1459-61del
XR_242246.3:n.3304-65_3304-61del (PEX1)
XM_017012319.2:c.1459-65_1459-61del (PEX1) XP_016867808.1:n.1459-65_1459-61del
XR_001744808.2:n.2235-65_2235-61del (PEX1)
XR_001744842.2:n.2602_2606del (GATAD1)
XR_001744843.2:n.2533_2537del (GATAD1)
XR_002956472.1:n.2659_2663del (GATAD1)
XR_002956473.1:n.2690_2694del (GATAD1)
XR_002956474.1:n.2607_2611del (GATAD1)
XR_242246.5:n.3255-65_3255-61del (PEX1)
XR_927494.3:n.1384_1388del (GATAD1)
XR_927500.3:n.1381_1385del (GATAD1)
XR_927503.3:n.1315_1319del (GATAD1)
NM_000466.3:c.3208-65_3208-61del (PEX1) MANE Select NP_000457.1:n.3208-65_3208-61del
NM_001282677.2:c.3037-65_3037-61del (PEX1) NP_001269606.1:n.3037-65_3037-61del
NM_001282678.2:c.2584-65_2584-61del (PEX1) NP_001269607.1:n.2584-65_2584-61del