Canonical Allele Identifier: CA368163518

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491319C>A , CM000669.2:g.92491319C>A GRCh38
NC_000007.13:g.92120633C>A , CM000669.1:g.92120633C>A GRCh37
NC_000007.12:g.91958569C>A NCBI36
NG_008341.1:g.42213G>T
NG_008341.2:g.42213G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3391G>T (PEX1) MANE Select ENSP00000248633.4:p.Gly1131Ter
ENST00000248633.8:c.3391G>T (PEX1) ENSP00000248633.4:p.Gly1131Ter
ENST00000428214.5:c.3220G>T (PEX1) ENSP00000394413.1:p.Gly1074Ter
ENST00000438045.5:c.2425G>T (PEX1) ENSP00000410438.1:p.Gly809Ter
ENST00000484913.5:n.3430G>T (PEX1)
ENST00000496420.5:n.4446G>T (PEX1)
NM_000466.2:c.3391G>T (PEX1) NP_000457.1:p.Gly1131Ter
NM_001282677.1:c.3220G>T (PEX1) NP_001269606.1:p.Gly1074Ter
NM_001282678.1:c.2767G>T (PEX1) NP_001269607.1:p.Gly923Ter
XM_005250433.3:c.1642G>T (PEX1) XP_005250490.1:p.Gly548Ter
XR_242246.3:n.3487G>T (PEX1)
XR_927494.1:n.1112C>A (GATAD1)
XR_927496.1:n.1117C>A (GATAD1)
XR_927497.1:n.1169C>A (GATAD1)
XR_927498.1:n.1200C>A (GATAD1)
XR_927500.1:n.1109C>A (GATAD1)
XR_927503.1:n.1043C>A (GATAD1)
XM_017012319.2:c.1642G>T (PEX1) XP_016867808.1:p.Gly548Ter
XR_001744808.2:n.2418G>T (PEX1)
XR_001744842.2:n.2357C>A (GATAD1)
XR_001744843.2:n.2288C>A (GATAD1)
XR_002956472.1:n.2414C>A (GATAD1)
XR_002956473.1:n.2445C>A (GATAD1)
XR_002956474.1:n.2362C>A (GATAD1)
XR_242246.5:n.3438G>T (PEX1)
XR_927494.3:n.1139C>A (GATAD1)
XR_927500.3:n.1136C>A (GATAD1)
XR_927503.3:n.1070C>A (GATAD1)
NM_000466.3:c.3391G>T (PEX1) MANE Select NP_000457.1:p.Gly1131Ter
NM_001282677.2:c.3220G>T (PEX1) NP_001269606.1:p.Gly1074Ter
NM_001282678.2:c.2767G>T (PEX1) NP_001269607.1:p.Gly923Ter