Canonical Allele Identifier: CA1725936117
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92501994T= , CM000669.2:g.92501994T= GRCh38
NC_000007.13:g.92131308T= , CM000669.1:g.92131308T= GRCh37
NC_000007.12:g.91969244T= NCBI36
NG_008341.1:g.31538A=
NG_008341.2:g.31538A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2312A= MANE Select ENSP00000248633.4:p.His771=
ENST00000248633.8:c.2312A= ENSP00000248633.4:p.His771=
ENST00000428214.5:c.2141A= ENSP00000394413.1:p.His714=
ENST00000438045.5:c.1346A= ENSP00000410438.1:p.His449=
ENST00000484913.5:n.2351A=
ENST00000496092.1:n.110A=
ENST00000496420.5:n.1988A=
NM_000466.2:c.2312A= NP_000457.1:p.His771=
NM_001282677.1:c.2141A= NP_001269606.1:p.His714=
NM_001282678.1:c.1688A= NP_001269607.1:p.His563=
XM_005250433.3:c.563A= XP_005250490.1:p.His188=
XR_242246.3:n.2408A=
XM_017012319.2:c.563A= XP_016867808.1:p.His188=
XR_001744808.2:n.1339A=
XR_242246.5:n.2359A=
NM_000466.3:c.2312A= MANE Select NP_000457.1:p.His771=
NM_001282677.2:c.2141A= NP_001269606.1:p.His714=
NM_001282678.2:c.1688A= NP_001269607.1:p.His563=