Canonical Allele Identifier: CA161973712
Gene: PEX1 HGNC NCBI

Linked Data

dbSNP Id: rs1023626342

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517796G>C , CM000669.2:g.92517796G>C GRCh38
NC_000007.13:g.92147110G>C , CM000669.1:g.92147110G>C GRCh37
NC_000007.12:g.91985046G>C NCBI36
NG_008341.1:g.15736C>G
NG_008341.2:g.15736C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.719C>G MANE Select ENSP00000248633.4:p.Ser240Ter
ENST00000248633.8:c.719C>G ENSP00000248633.4:p.Ser240Ter
ENST00000428214.5:c.719C>G ENSP00000394413.1:p.Ser240Ter
ENST00000438045.5:c.274-3829C>G ENSP00000410438.1:n.274-3829C>G
ENST00000484913.5:n.758C>G
NM_000466.2:c.719C>G NP_000457.1:p.Ser240Ter
NM_001282677.1:c.719C>G NP_001269606.1:p.Ser240Ter
NM_001282678.1:c.95C>G NP_001269607.1:p.Ser32Ter
XR_242246.3:n.815C>G
XR_242246.5:n.766C>G
NM_000466.3:c.719C>G MANE Select NP_000457.1:p.Ser240Ter
NM_001282677.2:c.719C>G NP_001269606.1:p.Ser240Ter
NM_001282678.2:c.95C>G NP_001269607.1:p.Ser32Ter