Canonical Allele Identifier: CA1725947073

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517137T= , CM000669.2:g.92517137T=	GRCh38
NC_000007.13:g.92146451T= , CM000669.1:g.92146451T=	GRCh37
NC_000007.12:g.91984387T=	NCBI36
NG_008341.1:g.16395A=
NG_008341.2:g.16395A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1239+139A= MANE Select	ENSP00000248633.4:n.1239+139A=
ENST00000248633.8:c.1239+139A=	ENSP00000248633.4:n.1239+139A=
ENST00000422866.1:c.140+139A=
ENST00000428214.5:c.1239+139A=	ENSP00000394413.1:n.1239+139A=
ENST00000438045.5:c.274-3170A=	ENSP00000410438.1:n.274-3170A=
ENST00000484913.5:n.1278+139A=
NM_000466.2:c.1239+139A=	NP_000457.1:n.1239+139A=
NM_001282677.1:c.1239+139A=	NP_001269606.1:n.1239+139A=
NM_001282678.1:c.615+139A=	NP_001269607.1:n.615+139A=
XR_242246.3:n.1335+139A=
XM_017012319.2:c.-428+139A=	XP_016867808.1:n.-428+139A=
XR_001744808.2:n.349+139A=
XR_242246.5:n.1286+139A=
NM_000466.3:c.1239+139A= MANE Select	NP_000457.1:n.1239+139A=
NM_001282677.2:c.1239+139A=	NP_001269606.1:n.1239+139A=
NM_001282678.2:c.615+139A=	NP_001269607.1:n.615+139A=