Canonical Allele Identifier: CA368167359

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494321T>G , CM000669.2:g.92494321T>G GRCh38
NC_000007.13:g.92123635T>G , CM000669.1:g.92123635T>G GRCh37
NC_000007.12:g.91961571T>G NCBI36
NG_008341.1:g.39211A>C
NG_008341.2:g.39211A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3002A>C (PEX1) MANE Select ENSP00000248633.4:p.Lys1001Thr
ENST00000248633.8:c.3002A>C (PEX1) ENSP00000248633.4:p.Lys1001Thr
ENST00000428214.5:c.2831A>C (PEX1) ENSP00000394413.1:p.Lys944Thr
ENST00000438045.5:c.2036A>C (PEX1) ENSP00000410438.1:p.Lys679Thr
ENST00000484913.5:n.3041A>C (PEX1)
ENST00000496420.5:n.2894A>C (PEX1)
NM_000466.2:c.3002A>C (PEX1) NP_000457.1:p.Lys1001Thr
NM_001282677.1:c.2831A>C (PEX1) NP_001269606.1:p.Lys944Thr
NM_001282678.1:c.2378A>C (PEX1) NP_001269607.1:p.Lys793Thr
XM_005250433.3:c.1253A>C (PEX1) XP_005250490.1:p.Lys418Thr
XR_242246.3:n.3098A>C (PEX1)
XM_017012319.2:c.1253A>C (PEX1) XP_016867808.1:p.Lys418Thr
XR_001744808.2:n.2029A>C (PEX1)
XR_001744843.2:n.5290T>G (GATAD1)
XR_242246.5:n.3049A>C (PEX1)
XR_927494.3:n.4141T>G (GATAD1)
XR_927503.3:n.4072T>G (GATAD1)
NM_000466.3:c.3002A>C (PEX1) MANE Select NP_000457.1:p.Lys1001Thr
NM_001282677.2:c.2831A>C (PEX1) NP_001269606.1:p.Lys944Thr
NM_001282678.2:c.2378A>C (PEX1) NP_001269607.1:p.Lys793Thr