Canonical Allele Identifier: CA368167312

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494306G>C , CM000669.2:g.92494306G>C GRCh38
NC_000007.13:g.92123620G>C , CM000669.1:g.92123620G>C GRCh37
NC_000007.12:g.91961556G>C NCBI36
NG_008341.1:g.39226C>G
NG_008341.2:g.39226C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3017C>G (PEX1) MANE Select ENSP00000248633.4:p.Pro1006Arg
ENST00000248633.8:c.3017C>G (PEX1) ENSP00000248633.4:p.Pro1006Arg
ENST00000428214.5:c.2846C>G (PEX1) ENSP00000394413.1:p.Pro949Arg
ENST00000438045.5:c.2051C>G (PEX1) ENSP00000410438.1:p.Pro684Arg
ENST00000484913.5:n.3056C>G (PEX1)
ENST00000496420.5:n.2909C>G (PEX1)
NM_000466.2:c.3017C>G (PEX1) NP_000457.1:p.Pro1006Arg
NM_001282677.1:c.2846C>G (PEX1) NP_001269606.1:p.Pro949Arg
NM_001282678.1:c.2393C>G (PEX1) NP_001269607.1:p.Pro798Arg
XM_005250433.3:c.1268C>G (PEX1) XP_005250490.1:p.Pro423Arg
XR_242246.3:n.3113C>G (PEX1)
XM_017012319.2:c.1268C>G (PEX1) XP_016867808.1:p.Pro423Arg
XR_001744808.2:n.2044C>G (PEX1)
XR_001744843.2:n.5275G>C (GATAD1)
XR_242246.5:n.3064C>G (PEX1)
XR_927494.3:n.4126G>C (GATAD1)
XR_927503.3:n.4057G>C (GATAD1)
NM_000466.3:c.3017C>G (PEX1) MANE Select NP_000457.1:p.Pro1006Arg
NM_001282677.2:c.2846C>G (PEX1) NP_001269606.1:p.Pro949Arg
NM_001282678.2:c.2393C>G (PEX1) NP_001269607.1:p.Pro798Arg