Canonical Allele Identifier: CA368167577

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494357A>C , CM000669.2:g.92494357A>C GRCh38
NC_000007.13:g.92123671A>C , CM000669.1:g.92123671A>C GRCh37
NC_000007.12:g.91961607A>C NCBI36
NG_008341.1:g.39175T>G
NG_008341.2:g.39175T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2966T>G (PEX1) MANE Select ENSP00000248633.4:p.Ile989Ser
ENST00000248633.8:c.2966T>G (PEX1) ENSP00000248633.4:p.Ile989Ser
ENST00000428214.5:c.2795T>G (PEX1) ENSP00000394413.1:p.Ile932Ser
ENST00000438045.5:c.2000T>G (PEX1) ENSP00000410438.1:p.Ile667Ser
ENST00000484913.5:n.3005T>G (PEX1)
ENST00000496420.5:n.2858T>G (PEX1)
NM_000466.2:c.2966T>G (PEX1) NP_000457.1:p.Ile989Ser
NM_001282677.1:c.2795T>G (PEX1) NP_001269606.1:p.Ile932Ser
NM_001282678.1:c.2342T>G (PEX1) NP_001269607.1:p.Ile781Ser
XM_005250433.3:c.1217T>G (PEX1) XP_005250490.1:p.Ile406Ser
XR_242246.3:n.3062T>G (PEX1)
XM_017012319.2:c.1217T>G (PEX1) XP_016867808.1:p.Ile406Ser
XR_001744808.2:n.1993T>G (PEX1)
XR_001744843.2:n.5326A>C (GATAD1)
XR_242246.5:n.3013T>G (PEX1)
XR_927494.3:n.4177A>C (GATAD1)
XR_927503.3:n.4108A>C (GATAD1)
NM_000466.3:c.2966T>G (PEX1) MANE Select NP_000457.1:p.Ile989Ser
NM_001282677.2:c.2795T>G (PEX1) NP_001269606.1:p.Ile932Ser
NM_001282678.2:c.2342T>G (PEX1) NP_001269607.1:p.Ile781Ser