Canonical Allele Identifier: CA1725947153

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517305C= , CM000669.2:g.92517305C=	GRCh38
NC_000007.13:g.92146619C= , CM000669.1:g.92146619C=	GRCh37
NC_000007.12:g.91984555C=	NCBI36
NG_008341.1:g.16227G=
NG_008341.2:g.16227G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1210G= MANE Select	ENSP00000248633.4:p.Val404=
ENST00000248633.8:c.1210G=	ENSP00000248633.4:p.Val404=
ENST00000422866.1:c.111G=
ENST00000428214.5:c.1210G=	ENSP00000394413.1:p.Val404=
ENST00000438045.5:c.274-3338G=	ENSP00000410438.1:n.274-3338G=
ENST00000484913.5:n.1249G=
NM_000466.2:c.1210G=	NP_000457.1:p.Val404=
NM_001282677.1:c.1210G=	NP_001269606.1:p.Val404=
NM_001282678.1:c.586G=	NP_001269607.1:p.Val196=
XR_242246.3:n.1306G=
XM_017012319.2:c.-457G=	XP_016867808.1:n.-457G=
XR_001744808.2:n.320G=
XR_242246.5:n.1257G=
NM_000466.3:c.1210G= MANE Select	NP_000457.1:p.Val404=
NM_001282677.2:c.1210G=	NP_001269606.1:p.Val404=
NM_001282678.2:c.586G=	NP_001269607.1:p.Val196=