Canonical Allele Identifier: CA1725938769

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504757C= , CM000669.2:g.92504757C=	GRCh38
NC_000007.13:g.92134071C= , CM000669.1:g.92134071C=	GRCh37
NC_000007.12:g.91972007C=	NCBI36
NG_008341.1:g.28775G=
NG_008341.2:g.28775G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2046G= MANE Select	ENSP00000248633.4:p.Ala682=
ENST00000248633.8:c.2046G=	ENSP00000248633.4:p.Ala682=
ENST00000428214.5:c.1900+1491G=	ENSP00000394413.1:n.1900+1491G=
ENST00000438045.5:c.1080G=	ENSP00000410438.1:p.Ala360=
ENST00000484913.5:n.2085G=
ENST00000496420.5:n.1722G=
NM_000466.2:c.2046G=	NP_000457.1:p.Ala682=
NM_001282677.1:c.1900+1491G=	NP_001269606.1:n.1900+1491G=
NM_001282678.1:c.1422G=	NP_001269607.1:p.Ala474=
XM_005250433.3:c.297G=	XP_005250490.1:p.Ala99=
XR_242246.3:n.2142G=
XM_017012319.2:c.297G=	XP_016867808.1:p.Ala99=
XR_001744808.2:n.1073G=
XR_242246.5:n.2093G=
NM_000466.3:c.2046G= MANE Select	NP_000457.1:p.Ala682=
NM_001282677.2:c.1900+1491G=	NP_001269606.1:n.1900+1491G=
NM_001282678.2:c.1422G=	NP_001269607.1:p.Ala474=