Canonical Allele Identifier: CA368198208
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517437G>T , CM000669.2:g.92517437G>T GRCh38
NC_000007.13:g.92146751G>T , CM000669.1:g.92146751G>T GRCh37
NC_000007.12:g.91984687G>T NCBI36
NG_008341.1:g.16095C>A
NG_008341.2:g.16095C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1078C>A MANE Select ENSP00000248633.4:p.Gln360Lys
ENST00000248633.8:c.1078C>A ENSP00000248633.4:p.Gln360Lys
ENST00000428214.5:c.1078C>A ENSP00000394413.1:p.Gln360Lys
ENST00000438045.5:c.274-3470C>A ENSP00000410438.1:n.274-3470C>A
ENST00000484913.5:n.1117C>A
NM_000466.2:c.1078C>A NP_000457.1:p.Gln360Lys
NM_001282677.1:c.1078C>A NP_001269606.1:p.Gln360Lys
NM_001282678.1:c.454C>A NP_001269607.1:p.Gln152Lys
XR_242246.3:n.1174C>A
XM_017012319.2:c.-589C>A XP_016867808.1:n.-589C>A
XR_001744808.2:n.188C>A
XR_242246.5:n.1125C>A
NM_000466.3:c.1078C>A MANE Select NP_000457.1:p.Gln360Lys
NM_001282677.2:c.1078C>A NP_001269606.1:p.Gln360Lys
NM_001282678.2:c.454C>A NP_001269607.1:p.Gln152Lys