Canonical Allele Identifier: CA4341574
Gene: PEX1 HGNC NCBI

Linked Data

dbSNP Id: rs749751537
gnomAD v2: 7-92147276-T-C
gnomAD v4: 7-92517962-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517962T>C , CM000669.2:g.92517962T>C GRCh38
NC_000007.13:g.92147276T>C , CM000669.1:g.92147276T>C GRCh37
NC_000007.12:g.91985212T>C NCBI36
NG_008341.1:g.15570A>G
NG_008341.2:g.15570A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.553A>G MANE Select ENSP00000248633.4:p.Lys185Glu
ENST00000248633.8:c.553A>G ENSP00000248633.4:p.Lys185Glu
ENST00000428214.5:c.553A>G ENSP00000394413.1:p.Lys185Glu
ENST00000438045.5:c.274-3995A>G ENSP00000410438.1:n.274-3995A>G
ENST00000484913.5:n.592A>G
NM_000466.2:c.553A>G NP_000457.1:p.Lys185Glu
NM_001282677.1:c.553A>G NP_001269606.1:p.Lys185Glu
NM_001282678.1:c.-72A>G NP_001269607.1:n.-72A>G
XR_242246.3:n.649A>G
XR_242246.5:n.600A>G
NM_000466.3:c.553A>G MANE Select NP_000457.1:p.Lys185Glu
NM_001282677.2:c.553A>G NP_001269606.1:p.Lys185Glu
NM_001282678.2:c.-72A>G NP_001269607.1:n.-72A>G