Canonical Allele Identifier: CA368164857

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491478C>A , CM000669.2:g.92491478C>A GRCh38
NC_000007.13:g.92120792C>A , CM000669.1:g.92120792C>A GRCh37
NC_000007.12:g.91958728C>A NCBI36
NG_008341.1:g.42054G>T
NG_008341.2:g.42054G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3232G>T (PEX1) MANE Select ENSP00000248633.4:p.Asp1078Tyr
ENST00000248633.8:c.3232G>T (PEX1) ENSP00000248633.4:p.Asp1078Tyr
ENST00000428214.5:c.3061G>T (PEX1) ENSP00000394413.1:p.Asp1021Tyr
ENST00000438045.5:c.2266G>T (PEX1) ENSP00000410438.1:p.Asp756Tyr
ENST00000484913.5:n.3271G>T (PEX1)
ENST00000496420.5:n.4287G>T (PEX1)
NM_000466.2:c.3232G>T (PEX1) NP_000457.1:p.Asp1078Tyr
NM_001282677.1:c.3061G>T (PEX1) NP_001269606.1:p.Asp1021Tyr
NM_001282678.1:c.2608G>T (PEX1) NP_001269607.1:p.Asp870Tyr
XM_005250433.3:c.1483G>T (PEX1) XP_005250490.1:p.Asp495Tyr
XR_242246.3:n.3328G>T (PEX1)
XM_017012319.2:c.1483G>T (PEX1) XP_016867808.1:p.Asp495Tyr
XR_001744808.2:n.2259G>T (PEX1)
XR_001744842.2:n.2516C>A (GATAD1)
XR_001744843.2:n.2447C>A (GATAD1)
XR_002956472.1:n.2573C>A (GATAD1)
XR_002956473.1:n.2604C>A (GATAD1)
XR_002956474.1:n.2521C>A (GATAD1)
XR_242246.5:n.3279G>T (PEX1)
XR_927494.3:n.1298C>A (GATAD1)
XR_927500.3:n.1295C>A (GATAD1)
XR_927503.3:n.1229C>A (GATAD1)
NM_000466.3:c.3232G>T (PEX1) MANE Select NP_000457.1:p.Asp1078Tyr
NM_001282677.2:c.3061G>T (PEX1) NP_001269606.1:p.Asp1021Tyr
NM_001282678.2:c.2608G>T (PEX1) NP_001269607.1:p.Asp870Tyr