Canonical Allele Identifier: CA368167352

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494319A>C , CM000669.2:g.92494319A>C GRCh38
NC_000007.13:g.92123633A>C , CM000669.1:g.92123633A>C GRCh37
NC_000007.12:g.91961569A>C NCBI36
NG_008341.1:g.39213T>G
NG_008341.2:g.39213T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3004T>G (PEX1) MANE Select ENSP00000248633.4:p.Cys1002Gly
ENST00000248633.8:c.3004T>G (PEX1) ENSP00000248633.4:p.Cys1002Gly
ENST00000428214.5:c.2833T>G (PEX1) ENSP00000394413.1:p.Cys945Gly
ENST00000438045.5:c.2038T>G (PEX1) ENSP00000410438.1:p.Cys680Gly
ENST00000484913.5:n.3043T>G (PEX1)
ENST00000496420.5:n.2896T>G (PEX1)
NM_000466.2:c.3004T>G (PEX1) NP_000457.1:p.Cys1002Gly
NM_001282677.1:c.2833T>G (PEX1) NP_001269606.1:p.Cys945Gly
NM_001282678.1:c.2380T>G (PEX1) NP_001269607.1:p.Cys794Gly
XM_005250433.3:c.1255T>G (PEX1) XP_005250490.1:p.Cys419Gly
XR_242246.3:n.3100T>G (PEX1)
XM_017012319.2:c.1255T>G (PEX1) XP_016867808.1:p.Cys419Gly
XR_001744808.2:n.2031T>G (PEX1)
XR_001744843.2:n.5288A>C (GATAD1)
XR_242246.5:n.3051T>G (PEX1)
XR_927494.3:n.4139A>C (GATAD1)
XR_927503.3:n.4070A>C (GATAD1)
NM_000466.3:c.3004T>G (PEX1) MANE Select NP_000457.1:p.Cys1002Gly
NM_001282677.2:c.2833T>G (PEX1) NP_001269606.1:p.Cys945Gly
NM_001282678.2:c.2380T>G (PEX1) NP_001269607.1:p.Cys794Gly