Canonical Allele Identifier: CA368203307
Gene: PEX1 HGNC NCBI

Linked Data

gnomAD v4: 7-92519069-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92519069T>G , CM000669.2:g.92519069T>G GRCh38
NC_000007.13:g.92148383T>G , CM000669.1:g.92148383T>G GRCh37
NC_000007.12:g.91986319T>G NCBI36
NG_008341.1:g.14463A>C
NG_008341.2:g.14463A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.283A>C MANE Select ENSP00000248633.4:p.Lys95Gln
ENST00000248633.8:c.283A>C ENSP00000248633.4:p.Lys95Gln
ENST00000428214.5:c.283A>C ENSP00000394413.1:p.Lys95Gln
ENST00000438045.5:c.273+3033A>C ENSP00000410438.1:n.273+3033A>C
ENST00000484913.5:n.287A>C
NM_000466.2:c.283A>C NP_000457.1:p.Lys95Gln
NM_001282677.1:c.283A>C NP_001269606.1:p.Lys95Gln
NM_001282678.1:c.-377A>C NP_001269607.1:n.-377A>C
XR_242246.3:n.379A>C
XR_242246.5:n.330A>C
NM_000466.3:c.283A>C MANE Select NP_000457.1:p.Lys95Gln
NM_001282677.2:c.283A>C NP_001269606.1:p.Lys95Gln
NM_001282678.2:c.-377A>C NP_001269607.1:n.-377A>C