Canonical Allele Identifier: CA1725936140

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92502037A= , CM000669.2:g.92502037A=	GRCh38
NC_000007.13:g.92131351A= , CM000669.1:g.92131351A=	GRCh37
NC_000007.12:g.91969287A=	NCBI36
NG_008341.1:g.31495T=
NG_008341.2:g.31495T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2269T= MANE Select	ENSP00000248633.4:p.Leu757=
ENST00000248633.8:c.2269T=	ENSP00000248633.4:p.Leu757=
ENST00000428214.5:c.2098T=	ENSP00000394413.1:p.Leu700=
ENST00000438045.5:c.1303T=	ENSP00000410438.1:p.Leu435=
ENST00000484913.5:n.2308T=
ENST00000496092.1:n.67T=
ENST00000496420.5:n.1945T=
NM_000466.2:c.2269T=	NP_000457.1:p.Leu757=
NM_001282677.1:c.2098T=	NP_001269606.1:p.Leu700=
NM_001282678.1:c.1645T=	NP_001269607.1:p.Leu549=
XM_005250433.3:c.520T=	XP_005250490.1:p.Leu174=
XR_242246.3:n.2365T=
XM_017012319.2:c.520T=	XP_016867808.1:p.Leu174=
XR_001744808.2:n.1296T=
XR_242246.5:n.2316T=
NM_000466.3:c.2269T= MANE Select	NP_000457.1:p.Leu757=
NM_001282677.2:c.2098T=	NP_001269606.1:p.Leu700=
NM_001282678.2:c.1645T=	NP_001269607.1:p.Leu549=