Canonical Allele Identifier: CA368160023

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489387T>G , CM000669.2:g.92489387T>G GRCh38
NC_000007.13:g.92118701T>G , CM000669.1:g.92118701T>G GRCh37
NC_000007.12:g.91956637T>G NCBI36
NG_008341.1:g.44145A>C
NG_008341.2:g.44145A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3673A>C (PEX1) MANE Select ENSP00000248633.4:p.Thr1225Pro
ENST00000248633.8:c.3673A>C (PEX1) ENSP00000248633.4:p.Thr1225Pro
ENST00000428214.5:c.3502A>C (PEX1) ENSP00000394413.1:p.Thr1168Pro
ENST00000438045.5:c.2707A>C (PEX1) ENSP00000410438.1:p.Thr903Pro
ENST00000469417.1:n.570A>C (PEX1)
ENST00000477342.1:n.408A>C (PEX1)
ENST00000484913.5:n.3712A>C (PEX1)
ENST00000496420.5:n.4723A>C (PEX1)
NM_000466.2:c.3673A>C (PEX1) NP_000457.1:p.Thr1225Pro
NM_001282677.1:c.3502A>C (PEX1) NP_001269606.1:p.Thr1168Pro
NM_001282678.1:c.3049A>C (PEX1) NP_001269607.1:p.Thr1017Pro
XM_005250433.3:c.1924A>C (PEX1) XP_005250490.1:p.Thr642Pro
XR_242246.3:n.3764A>C (PEX1)
XR_927494.1:n.1036-1856T>G (GATAD1)
XR_927495.1:n.1036-699T>G (GATAD1)
XR_927496.1:n.1041-1856T>G (GATAD1)
XR_927497.1:n.1036-699T>G (GATAD1)
XR_927498.1:n.1124-1856T>G (GATAD1)
XR_927500.1:n.1033-1856T>G (GATAD1)
XR_927502.1:n.1033-699T>G (GATAD1)
XR_927503.1:n.967-1856T>G (GATAD1)
XM_017012319.2:c.1924A>C (PEX1) XP_016867808.1:p.Thr642Pro
XR_001744808.2:n.2695A>C (PEX1)
XR_001744842.2:n.2281-1856T>G (GATAD1)
XR_001744843.2:n.2212-1856T>G (GATAD1)
XR_002956472.1:n.2281-699T>G (GATAD1)
XR_002956473.1:n.2369-1856T>G (GATAD1)
XR_002956474.1:n.2286-1856T>G (GATAD1)
XR_242246.5:n.3715A>C (PEX1)
XR_927494.3:n.1063-1856T>G (GATAD1)
XR_927500.3:n.1060-1856T>G (GATAD1)
XR_927503.3:n.994-1856T>G (GATAD1)
NM_000466.3:c.3673A>C (PEX1) MANE Select NP_000457.1:p.Thr1225Pro
NM_001282677.2:c.3502A>C (PEX1) NP_001269606.1:p.Thr1168Pro
NM_001282678.2:c.3049A>C (PEX1) NP_001269607.1:p.Thr1017Pro