Canonical Allele Identifier: CA161953238

Linked Data

dbSNP Id: rs1027772532

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491492G>A , CM000669.2:g.92491492G>A GRCh38
NC_000007.13:g.92120806G>A , CM000669.1:g.92120806G>A GRCh37
NC_000007.12:g.91958742G>A NCBI36
NG_008341.1:g.42040C>T
NG_008341.2:g.42040C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3218C>T (PEX1) MANE Select ENSP00000248633.4:p.Ser1073Phe
ENST00000248633.8:c.3218C>T (PEX1) ENSP00000248633.4:p.Ser1073Phe
ENST00000428214.5:c.3047C>T (PEX1) ENSP00000394413.1:p.Ser1016Phe
ENST00000438045.5:c.2252C>T (PEX1) ENSP00000410438.1:p.Ser751Phe
ENST00000484913.5:n.3257C>T (PEX1)
ENST00000496420.5:n.4273C>T (PEX1)
NM_000466.2:c.3218C>T (PEX1) NP_000457.1:p.Ser1073Phe
NM_001282677.1:c.3047C>T (PEX1) NP_001269606.1:p.Ser1016Phe
NM_001282678.1:c.2594C>T (PEX1) NP_001269607.1:p.Ser865Phe
XM_005250433.3:c.1469C>T (PEX1) XP_005250490.1:p.Ser490Phe
XR_242246.3:n.3314C>T (PEX1)
XM_017012319.2:c.1469C>T (PEX1) XP_016867808.1:p.Ser490Phe
XR_001744808.2:n.2245C>T (PEX1)
XR_001744842.2:n.2530G>A (GATAD1)
XR_001744843.2:n.2461G>A (GATAD1)
XR_002956472.1:n.2587G>A (GATAD1)
XR_002956473.1:n.2618G>A (GATAD1)
XR_002956474.1:n.2535G>A (GATAD1)
XR_242246.5:n.3265C>T (PEX1)
XR_927494.3:n.1312G>A (GATAD1)
XR_927500.3:n.1309G>A (GATAD1)
XR_927503.3:n.1243G>A (GATAD1)
NM_000466.3:c.3218C>T (PEX1) MANE Select NP_000457.1:p.Ser1073Phe
NM_001282677.2:c.3047C>T (PEX1) NP_001269606.1:p.Ser1016Phe
NM_001282678.2:c.2594C>T (PEX1) NP_001269607.1:p.Ser865Phe