Canonical Allele Identifier: CA1725933332

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496734G= , CM000669.2:g.92496734G=	GRCh38
NC_000007.13:g.92126048G= , CM000669.1:g.92126048G=	GRCh37
NC_000007.12:g.91963984G=	NCBI36
NG_008341.1:g.36798C=
NG_008341.2:g.36798C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2762C= MANE Select	ENSP00000248633.4:p.Ala921=
ENST00000248633.8:c.2762C=	ENSP00000248633.4:p.Ala921=
ENST00000428214.5:c.2591C=	ENSP00000394413.1:p.Ala864=
ENST00000438045.5:c.1796C=	ENSP00000410438.1:p.Ala599=
ENST00000484913.5:n.2801C=
ENST00000496420.5:n.2654C=
NM_000466.2:c.2762C=	NP_000457.1:p.Ala921=
NM_001282677.1:c.2591C=	NP_001269606.1:p.Ala864=
NM_001282678.1:c.2138C=	NP_001269607.1:p.Ala713=
XM_005250433.3:c.1013C=	XP_005250490.1:p.Ala338=
XR_242246.3:n.2858C=
XM_017012319.2:c.1013C=	XP_016867808.1:p.Ala338=
XR_001744808.2:n.1789C=
XR_242246.5:n.2809C=
NM_000466.3:c.2762C= MANE Select	NP_000457.1:p.Ala921=
NM_001282677.2:c.2591C=	NP_001269606.1:p.Ala864=
NM_001282678.2:c.2138C=	NP_001269607.1:p.Ala713=