Canonical Allele Identifier: CA368185266
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92506320T>G , CM000669.2:g.92506320T>G GRCh38
NC_000007.13:g.92135634T>G , CM000669.1:g.92135634T>G GRCh37
NC_000007.12:g.91973570T>G NCBI36
NG_008341.1:g.27212A>C
NG_008341.2:g.27212A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.1828A>C MANE Select ENSP00000248633.4:p.Lys610Gln
ENST00000248633.8:c.1828A>C ENSP00000248633.4:p.Lys610Gln
ENST00000422866.1:c.646A>C
ENST00000428214.5:c.1828A>C ENSP00000394413.1:p.Lys610Gln
ENST00000438045.5:c.862A>C ENSP00000410438.1:p.Lys288Gln
ENST00000484913.5:n.1867A>C
ENST00000496420.5:n.1504A>C
NM_000466.2:c.1828A>C NP_000457.1:p.Lys610Gln
NM_001282677.1:c.1828A>C NP_001269606.1:p.Lys610Gln
NM_001282678.1:c.1204A>C NP_001269607.1:p.Lys402Gln
XM_005250433.3:c.79A>C XP_005250490.1:p.Lys27Gln
XR_242246.3:n.1924A>C
XM_017012319.2:c.79A>C XP_016867808.1:p.Lys27Gln
XR_001744808.2:n.855A>C
XR_242246.5:n.1875A>C
NM_000466.3:c.1828A>C MANE Select NP_000457.1:p.Lys610Gln
NM_001282677.2:c.1828A>C NP_001269606.1:p.Lys610Gln
NM_001282678.2:c.1204A>C NP_001269607.1:p.Lys402Gln