Canonical Allele Identifier: CA1725947077

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517140G= , CM000669.2:g.92517140G=	GRCh38
NC_000007.13:g.92146454G= , CM000669.1:g.92146454G=	GRCh37
NC_000007.12:g.91984390G=	NCBI36
NG_008341.1:g.16392C=
NG_008341.2:g.16392C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1239+136C= MANE Select	ENSP00000248633.4:n.1239+136C=
ENST00000248633.8:c.1239+136C=	ENSP00000248633.4:n.1239+136C=
ENST00000422866.1:c.140+136C=
ENST00000428214.5:c.1239+136C=	ENSP00000394413.1:n.1239+136C=
ENST00000438045.5:c.274-3173C=	ENSP00000410438.1:n.274-3173C=
ENST00000484913.5:n.1278+136C=
NM_000466.2:c.1239+136C=	NP_000457.1:n.1239+136C=
NM_001282677.1:c.1239+136C=	NP_001269606.1:n.1239+136C=
NM_001282678.1:c.615+136C=	NP_001269607.1:n.615+136C=
XR_242246.3:n.1335+136C=
XM_017012319.2:c.-428+136C=	XP_016867808.1:n.-428+136C=
XR_001744808.2:n.349+136C=
XR_242246.5:n.1286+136C=
NM_000466.3:c.1239+136C= MANE Select	NP_000457.1:n.1239+136C=
NM_001282677.2:c.1239+136C=	NP_001269606.1:n.1239+136C=
NM_001282678.2:c.615+136C=	NP_001269607.1:n.615+136C=