Canonical Allele Identifier: CA1725933253
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92496674C= , CM000669.2:g.92496674C= GRCh38
NC_000007.13:g.92125988C= , CM000669.1:g.92125988C= GRCh37
NC_000007.12:g.91963924C= NCBI36
NG_008341.1:g.36858G=
NG_008341.2:g.36858G=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2783+39G= MANE Select ENSP00000248633.4:n.2783+39G=
ENST00000248633.8:c.2783+39G= ENSP00000248633.4:n.2783+39G=
ENST00000428214.5:c.2612+39G= ENSP00000394413.1:n.2612+39G=
ENST00000438045.5:c.1817+39G= ENSP00000410438.1:n.1817+39G=
ENST00000484913.5:n.2822+39G=
ENST00000496420.5:n.2675+39G=
NM_000466.2:c.2783+39G= NP_000457.1:n.2783+39G=
NM_001282677.1:c.2612+39G= NP_001269606.1:n.2612+39G=
NM_001282678.1:c.2159+39G= NP_001269607.1:n.2159+39G=
XM_005250433.3:c.1034+39G= XP_005250490.1:n.1034+39G=
XR_242246.3:n.2879+39G=
XM_017012319.2:c.1034+39G= XP_016867808.1:n.1034+39G=
XR_001744808.2:n.1810+39G=
XR_242246.5:n.2830+39G=
NM_000466.3:c.2783+39G= MANE Select NP_000457.1:n.2783+39G=
NM_001282677.2:c.2612+39G= NP_001269606.1:n.2612+39G=
NM_001282678.2:c.2159+39G= NP_001269607.1:n.2159+39G=