Canonical Allele Identifier: CA368168523

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494543G>T , CM000669.2:g.92494543G>T GRCh38
NC_000007.13:g.92123857G>T , CM000669.1:g.92123857G>T GRCh37
NC_000007.12:g.91961793G>T NCBI36
NG_008341.1:g.38989C>A
NG_008341.2:g.38989C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2870C>A (PEX1) MANE Select ENSP00000248633.4:p.Thr957Lys
ENST00000248633.8:c.2870C>A (PEX1) ENSP00000248633.4:p.Thr957Lys
ENST00000428214.5:c.2699C>A (PEX1) ENSP00000394413.1:p.Thr900Lys
ENST00000438045.5:c.1904C>A (PEX1) ENSP00000410438.1:p.Thr635Lys
ENST00000484913.5:n.2909C>A (PEX1)
ENST00000496420.5:n.2762C>A (PEX1)
NM_000466.2:c.2870C>A (PEX1) NP_000457.1:p.Thr957Lys
NM_001282677.1:c.2699C>A (PEX1) NP_001269606.1:p.Thr900Lys
NM_001282678.1:c.2246C>A (PEX1) NP_001269607.1:p.Thr749Lys
XM_005250433.3:c.1121C>A (PEX1) XP_005250490.1:p.Thr374Lys
XR_242246.3:n.2966C>A (PEX1)
XM_017012319.2:c.1121C>A (PEX1) XP_016867808.1:p.Thr374Lys
XR_001744808.2:n.1897C>A (PEX1)
XR_001744843.2:n.5512G>T (GATAD1)
XR_242246.5:n.2917C>A (PEX1)
XR_927494.3:n.4363G>T (GATAD1)
XR_927503.3:n.4294G>T (GATAD1)
NM_000466.3:c.2870C>A (PEX1) MANE Select NP_000457.1:p.Thr957Lys
NM_001282677.2:c.2699C>A (PEX1) NP_001269606.1:p.Thr900Lys
NM_001282678.2:c.2246C>A (PEX1) NP_001269607.1:p.Thr749Lys