Canonical Allele Identifier: CA843844298

Linked Data

dbSNP Id: rs1223783841

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489678G>A , CM000669.2:g.92489678G>A GRCh38
NC_000007.13:g.92118992G>A , CM000669.1:g.92118992G>A GRCh37
NC_000007.12:g.91956928G>A NCBI36
NG_008341.1:g.43854C>T
NG_008341.2:g.43854C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3636+36C>T (PEX1) MANE Select ENSP00000248633.4:n.3636+36C>T
ENST00000248633.8:c.3636+36C>T (PEX1) ENSP00000248633.4:n.3636+36C>T
ENST00000428214.5:c.3465+36C>T (PEX1) ENSP00000394413.1:n.3465+36C>T
ENST00000438045.5:c.2670+36C>T (PEX1) ENSP00000410438.1:n.2670+36C>T
ENST00000469417.1:n.533+36C>T (PEX1)
ENST00000477342.1:n.117C>T (PEX1)
ENST00000484913.5:n.3675+36C>T (PEX1)
ENST00000496420.5:n.4686+41C>T (PEX1)
NM_000466.2:c.3636+36C>T (PEX1) NP_000457.1:n.3636+36C>T
NM_001282677.1:c.3465+36C>T (PEX1) NP_001269606.1:n.3465+36C>T
NM_001282678.1:c.3012+36C>T (PEX1) NP_001269607.1:n.3012+36C>T
XM_005250433.3:c.1887+36C>T (PEX1) XP_005250490.1:n.1887+36C>T
XR_242246.3:n.3727+41C>T (PEX1)
XR_927494.1:n.1036-1565G>A (GATAD1)
XR_927495.1:n.1036-408G>A (GATAD1)
XR_927496.1:n.1041-1565G>A (GATAD1)
XR_927497.1:n.1036-408G>A (GATAD1)
XR_927498.1:n.1124-1565G>A (GATAD1)
XR_927500.1:n.1033-1565G>A (GATAD1)
XR_927502.1:n.1033-408G>A (GATAD1)
XR_927503.1:n.967-1565G>A (GATAD1)
XM_017012319.2:c.1887+36C>T (PEX1) XP_016867808.1:n.1887+36C>T
XR_001744808.2:n.2658+41C>T (PEX1)
XR_001744842.2:n.2281-1565G>A (GATAD1)
XR_001744843.2:n.2212-1565G>A (GATAD1)
XR_002956472.1:n.2281-408G>A (GATAD1)
XR_002956473.1:n.2369-1565G>A (GATAD1)
XR_002956474.1:n.2286-1565G>A (GATAD1)
XR_242246.5:n.3678+41C>T (PEX1)
XR_927494.3:n.1063-1565G>A (GATAD1)
XR_927500.3:n.1060-1565G>A (GATAD1)
XR_927503.3:n.994-1565G>A (GATAD1)
NM_000466.3:c.3636+36C>T (PEX1) MANE Select NP_000457.1:n.3636+36C>T
NM_001282677.2:c.3465+36C>T (PEX1) NP_001269606.1:n.3465+36C>T
NM_001282678.2:c.3012+36C>T (PEX1) NP_001269607.1:n.3012+36C>T