Canonical Allele Identifier: CA1725949222

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518954T= , CM000669.2:g.92518954T=	GRCh38
NC_000007.13:g.92148268T= , CM000669.1:g.92148268T=	GRCh37
NC_000007.12:g.91986204T=	NCBI36
NG_008341.1:g.14578A=
NG_008341.2:g.14578A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.357+41A= MANE Select	ENSP00000248633.4:n.357+41A=
ENST00000248633.8:c.357+41A=	ENSP00000248633.4:n.357+41A=
ENST00000428214.5:c.357+41A=	ENSP00000394413.1:n.357+41A=
ENST00000438045.5:c.273+3148A=	ENSP00000410438.1:n.273+3148A=
ENST00000484913.5:n.396+6A=
NM_000466.2:c.357+41A=	NP_000457.1:n.357+41A=
NM_001282677.1:c.357+41A=	NP_001269606.1:n.357+41A=
NM_001282678.1:c.-268+6A=	NP_001269607.1:n.-268+6A=
XR_242246.3:n.453+41A=
XR_242246.5:n.404+41A=
NM_000466.3:c.357+41A= MANE Select	NP_000457.1:n.357+41A=
NM_001282677.2:c.357+41A=	NP_001269606.1:n.357+41A=
NM_001282678.2:c.-268+6A=	NP_001269607.1:n.-268+6A=