Canonical Allele Identifier: CA1725928680

Linked Data

dbSNP Id: rs1791325213

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491572_92491573del , CM000669.2:g.92491572_92491573del GRCh38
NC_000007.13:g.92120886_92120887del , CM000669.1:g.92120886_92120887del GRCh37
NC_000007.12:g.91958822_91958823del NCBI36
NG_008341.1:g.41960_41961del
NG_008341.2:g.41960_41961del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3208-70_3208-69del (PEX1) MANE Select ENSP00000248633.4:n.3208-70_3208-69del
ENST00000248633.8:c.3208-70_3208-69del (PEX1) ENSP00000248633.4:n.3208-70_3208-69del
ENST00000428214.5:c.3037-70_3037-69del (PEX1) ENSP00000394413.1:n.3037-70_3037-69del
ENST00000438045.5:c.2242-70_2242-69del (PEX1) ENSP00000410438.1:n.2242-70_2242-69del
ENST00000484913.5:n.3247-70_3247-69del (PEX1)
ENST00000496420.5:n.4263-70_4263-69del (PEX1)
NM_000466.2:c.3208-70_3208-69del (PEX1) NP_000457.1:n.3208-70_3208-69del
NM_001282677.1:c.3037-70_3037-69del (PEX1) NP_001269606.1:n.3037-70_3037-69del
NM_001282678.1:c.2584-70_2584-69del (PEX1) NP_001269607.1:n.2584-70_2584-69del
XM_005250433.3:c.1459-70_1459-69del (PEX1) XP_005250490.1:n.1459-70_1459-69del
XR_242246.3:n.3304-70_3304-69del (PEX1)
XM_017012319.2:c.1459-70_1459-69del (PEX1) XP_016867808.1:n.1459-70_1459-69del
XR_001744808.2:n.2235-70_2235-69del (PEX1)
XR_001744842.2:n.2610_2611del (GATAD1)
XR_001744843.2:n.2541_2542del (GATAD1)
XR_002956472.1:n.2667_2668del (GATAD1)
XR_002956473.1:n.2698_2699del (GATAD1)
XR_002956474.1:n.2615_2616del (GATAD1)
XR_242246.5:n.3255-70_3255-69del (PEX1)
XR_927494.3:n.1392_1393del (GATAD1)
XR_927500.3:n.1389_1390del (GATAD1)
XR_927503.3:n.1323_1324del (GATAD1)
NM_000466.3:c.3208-70_3208-69del (PEX1) MANE Select NP_000457.1:n.3208-70_3208-69del
NM_001282677.2:c.3037-70_3037-69del (PEX1) NP_001269606.1:n.3037-70_3037-69del
NM_001282678.2:c.2584-70_2584-69del (PEX1) NP_001269607.1:n.2584-70_2584-69del