Canonical Allele Identifier: CA1725941831

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506881T= , CM000669.2:g.92506881T=	GRCh38
NC_000007.13:g.92136195T= , CM000669.1:g.92136195T=	GRCh37
NC_000007.12:g.91974131T=	NCBI36
NG_008341.1:g.26651A=
NG_008341.2:g.26651A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1803+113A= MANE Select	ENSP00000248633.4:n.1803+113A=
ENST00000248633.8:c.1803+113A=	ENSP00000248633.4:n.1803+113A=
ENST00000422866.1:c.621+113A=
ENST00000428214.5:c.1803+113A=	ENSP00000394413.1:n.1803+113A=
ENST00000438045.5:c.837+113A=	ENSP00000410438.1:n.837+113A=
ENST00000484913.5:n.1842+113A=
ENST00000496420.5:n.943A=
NM_000466.2:c.1803+113A=	NP_000457.1:n.1803+113A=
NM_001282677.1:c.1803+113A=	NP_001269606.1:n.1803+113A=
NM_001282678.1:c.1179+113A=	NP_001269607.1:n.1179+113A=
XM_005250433.3:c.54+113A=	XP_005250490.1:n.54+113A=
XR_242246.3:n.1899+113A=
XM_017012319.2:c.54+113A=	XP_016867808.1:n.54+113A=
XR_001744808.2:n.830+113A=
XR_242246.5:n.1850+113A=
NM_000466.3:c.1803+113A= MANE Select	NP_000457.1:n.1803+113A=
NM_001282677.2:c.1803+113A=	NP_001269606.1:n.1803+113A=
NM_001282678.2:c.1179+113A=	NP_001269607.1:n.1179+113A=