Canonical Allele Identifier: CA368167639

Linked Data

gnomAD v4: 7-92494367-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494367G>A , CM000669.2:g.92494367G>A GRCh38
NC_000007.13:g.92123681G>A , CM000669.1:g.92123681G>A GRCh37
NC_000007.12:g.91961617G>A NCBI36
NG_008341.1:g.39165C>T
NG_008341.2:g.39165C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2956C>T (PEX1) MANE Select ENSP00000248633.4:p.Pro986Ser
ENST00000248633.8:c.2956C>T (PEX1) ENSP00000248633.4:p.Pro986Ser
ENST00000428214.5:c.2785C>T (PEX1) ENSP00000394413.1:p.Pro929Ser
ENST00000438045.5:c.1990C>T (PEX1) ENSP00000410438.1:p.Pro664Ser
ENST00000484913.5:n.2995C>T (PEX1)
ENST00000496420.5:n.2848C>T (PEX1)
NM_000466.2:c.2956C>T (PEX1) NP_000457.1:p.Pro986Ser
NM_001282677.1:c.2785C>T (PEX1) NP_001269606.1:p.Pro929Ser
NM_001282678.1:c.2332C>T (PEX1) NP_001269607.1:p.Pro778Ser
XM_005250433.3:c.1207C>T (PEX1) XP_005250490.1:p.Pro403Ser
XR_242246.3:n.3052C>T (PEX1)
XM_017012319.2:c.1207C>T (PEX1) XP_016867808.1:p.Pro403Ser
XR_001744808.2:n.1983C>T (PEX1)
XR_001744843.2:n.5336G>A (GATAD1)
XR_242246.5:n.3003C>T (PEX1)
XR_927494.3:n.4187G>A (GATAD1)
XR_927503.3:n.4118G>A (GATAD1)
NM_000466.3:c.2956C>T (PEX1) MANE Select NP_000457.1:p.Pro986Ser
NM_001282677.2:c.2785C>T (PEX1) NP_001269606.1:p.Pro929Ser
NM_001282678.2:c.2332C>T (PEX1) NP_001269607.1:p.Pro778Ser