Canonical Allele Identifier: CA368202313
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518195T>G , CM000669.2:g.92518195T>G GRCh38
NC_000007.13:g.92147509T>G , CM000669.1:g.92147509T>G GRCh37
NC_000007.12:g.91985445T>G NCBI36
NG_008341.1:g.15337A>C
NG_008341.2:g.15337A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.418A>C MANE Select ENSP00000248633.4:p.Lys140Gln
ENST00000248633.8:c.418A>C ENSP00000248633.4:p.Lys140Gln
ENST00000428214.5:c.418A>C ENSP00000394413.1:p.Lys140Gln
ENST00000438045.5:c.273+3907A>C ENSP00000410438.1:n.273+3907A>C
ENST00000484913.5:n.457A>C
NM_000466.2:c.418A>C NP_000457.1:p.Lys140Gln
NM_001282677.1:c.418A>C NP_001269606.1:p.Lys140Gln
NM_001282678.1:c.-207A>C NP_001269607.1:n.-207A>C
XR_242246.3:n.514A>C
XR_242246.5:n.465A>C
NM_000466.3:c.418A>C MANE Select NP_000457.1:p.Lys140Gln
NM_001282677.2:c.418A>C NP_001269606.1:p.Lys140Gln
NM_001282678.2:c.-207A>C NP_001269607.1:n.-207A>C