Canonical Allele Identifier: CA1725941210

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506314T= , CM000669.2:g.92506314T=	GRCh38
NC_000007.13:g.92135628T= , CM000669.1:g.92135628T=	GRCh37
NC_000007.12:g.91973564T=	NCBI36
NG_008341.1:g.27218A=
NG_008341.2:g.27218A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1834A= MANE Select	ENSP00000248633.4:p.Ile612=
ENST00000248633.8:c.1834A=	ENSP00000248633.4:p.Ile612=
ENST00000422866.1:c.652A=
ENST00000428214.5:c.1834A=	ENSP00000394413.1:p.Ile612=
ENST00000438045.5:c.868A=	ENSP00000410438.1:p.Ile290=
ENST00000484913.5:n.1873A=
ENST00000496420.5:n.1510A=
NM_000466.2:c.1834A=	NP_000457.1:p.Ile612=
NM_001282677.1:c.1834A=	NP_001269606.1:p.Ile612=
NM_001282678.1:c.1210A=	NP_001269607.1:p.Ile404=
XM_005250433.3:c.85A=	XP_005250490.1:p.Ile29=
XR_242246.3:n.1930A=
XM_017012319.2:c.85A=	XP_016867808.1:p.Ile29=
XR_001744808.2:n.861A=
XR_242246.5:n.1881A=
NM_000466.3:c.1834A= MANE Select	NP_000457.1:p.Ile612=
NM_001282677.2:c.1834A=	NP_001269606.1:p.Ile612=
NM_001282678.2:c.1210A=	NP_001269607.1:p.Ile404=