Canonical Allele Identifier: CA368200589
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517848C>T , CM000669.2:g.92517848C>T GRCh38
NC_000007.13:g.92147162C>T , CM000669.1:g.92147162C>T GRCh37
NC_000007.12:g.91985098C>T NCBI36
NG_008341.1:g.15684G>A
NG_008341.2:g.15684G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.667G>A MANE Select ENSP00000248633.4:p.Val223Met
ENST00000248633.8:c.667G>A ENSP00000248633.4:p.Val223Met
ENST00000428214.5:c.667G>A ENSP00000394413.1:p.Val223Met
ENST00000438045.5:c.274-3881G>A ENSP00000410438.1:n.274-3881G>A
ENST00000484913.5:n.706G>A
NM_000466.2:c.667G>A NP_000457.1:p.Val223Met
NM_001282677.1:c.667G>A NP_001269606.1:p.Val223Met
NM_001282678.1:c.43G>A NP_001269607.1:p.Val15Met
XR_242246.3:n.763G>A
XR_242246.5:n.714G>A
NM_000466.3:c.667G>A MANE Select NP_000457.1:p.Val223Met
NM_001282677.2:c.667G>A NP_001269606.1:p.Val223Met
NM_001282678.2:c.43G>A NP_001269607.1:p.Val15Met