Canonical Allele Identifier: CA368167626

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494363T>A , CM000669.2:g.92494363T>A GRCh38
NC_000007.13:g.92123677T>A , CM000669.1:g.92123677T>A GRCh37
NC_000007.12:g.91961613T>A NCBI36
NG_008341.1:g.39169A>T
NG_008341.2:g.39169A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2960A>T (PEX1) MANE Select ENSP00000248633.4:p.Asp987Val
ENST00000248633.8:c.2960A>T (PEX1) ENSP00000248633.4:p.Asp987Val
ENST00000428214.5:c.2789A>T (PEX1) ENSP00000394413.1:p.Asp930Val
ENST00000438045.5:c.1994A>T (PEX1) ENSP00000410438.1:p.Asp665Val
ENST00000484913.5:n.2999A>T (PEX1)
ENST00000496420.5:n.2852A>T (PEX1)
NM_000466.2:c.2960A>T (PEX1) NP_000457.1:p.Asp987Val
NM_001282677.1:c.2789A>T (PEX1) NP_001269606.1:p.Asp930Val
NM_001282678.1:c.2336A>T (PEX1) NP_001269607.1:p.Asp779Val
XM_005250433.3:c.1211A>T (PEX1) XP_005250490.1:p.Asp404Val
XR_242246.3:n.3056A>T (PEX1)
XM_017012319.2:c.1211A>T (PEX1) XP_016867808.1:p.Asp404Val
XR_001744808.2:n.1987A>T (PEX1)
XR_001744843.2:n.5332T>A (GATAD1)
XR_242246.5:n.3007A>T (PEX1)
XR_927494.3:n.4183T>A (GATAD1)
XR_927503.3:n.4114T>A (GATAD1)
NM_000466.3:c.2960A>T (PEX1) MANE Select NP_000457.1:p.Asp987Val
NM_001282677.2:c.2789A>T (PEX1) NP_001269606.1:p.Asp930Val
NM_001282678.2:c.2336A>T (PEX1) NP_001269607.1:p.Asp779Val