Canonical Allele Identifier: CA1725948066

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517889A= , CM000669.2:g.92517889A=	GRCh38
NC_000007.13:g.92147203A= , CM000669.1:g.92147203A=	GRCh37
NC_000007.12:g.91985139A=	NCBI36
NG_008341.1:g.15643T=
NG_008341.2:g.15643T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.626T= MANE Select	ENSP00000248633.4:p.Met209=
ENST00000248633.8:c.626T=	ENSP00000248633.4:p.Met209=
ENST00000428214.5:c.626T=	ENSP00000394413.1:p.Met209=
ENST00000438045.5:c.274-3922T=	ENSP00000410438.1:n.274-3922T=
ENST00000484913.5:n.665T=
NM_000466.2:c.626T=	NP_000457.1:p.Met209=
NM_001282677.1:c.626T=	NP_001269606.1:p.Met209=
NM_001282678.1:c.2T=	NP_001269607.1:p.Met1=
XR_242246.3:n.722T=
XR_242246.5:n.673T=
NM_000466.3:c.626T= MANE Select	NP_000457.1:p.Met209=
NM_001282677.2:c.626T=	NP_001269606.1:p.Met209=
NM_001282678.2:c.2T=	NP_001269607.1:p.Met1=