Canonical Allele Identifier: CA1104476443
Gene: PEX1 HGNC NCBI

Linked Data

dbSNP Id: rs1792827376
gnomAD v3: 7-92517173-T-A
gnomAD v4: 7-92517173-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517173T>A , CM000669.2:g.92517173T>A GRCh38
NC_000007.13:g.92146487T>A , CM000669.1:g.92146487T>A GRCh37
NC_000007.12:g.91984423T>A NCBI36
NG_008341.1:g.16359A>T
NG_008341.2:g.16359A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1239+103A>T MANE Select ENSP00000248633.4:n.1239+103A>T
ENST00000248633.8:c.1239+103A>T ENSP00000248633.4:n.1239+103A>T
ENST00000422866.1:c.140+103A>T
ENST00000428214.5:c.1239+103A>T ENSP00000394413.1:n.1239+103A>T
ENST00000438045.5:c.274-3206A>T ENSP00000410438.1:n.274-3206A>T
ENST00000484913.5:n.1278+103A>T
NM_000466.2:c.1239+103A>T NP_000457.1:n.1239+103A>T
NM_001282677.1:c.1239+103A>T NP_001269606.1:n.1239+103A>T
NM_001282678.1:c.615+103A>T NP_001269607.1:n.615+103A>T
XR_242246.3:n.1335+103A>T
XM_017012319.2:c.-428+103A>T XP_016867808.1:n.-428+103A>T
XR_001744808.2:n.349+103A>T
XR_242246.5:n.1286+103A>T
NM_000466.3:c.1239+103A>T MANE Select NP_000457.1:n.1239+103A>T
NM_001282677.2:c.1239+103A>T NP_001269606.1:n.1239+103A>T
NM_001282678.2:c.615+103A>T NP_001269607.1:n.615+103A>T