Canonical Allele Identifier: CA1725949262

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518989C= , CM000669.2:g.92518989C=	GRCh38
NC_000007.13:g.92148303C= , CM000669.1:g.92148303C=	GRCh37
NC_000007.12:g.91986239C=	NCBI36
NG_008341.1:g.14543G=
NG_008341.2:g.14543G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.357+6G= MANE Select	ENSP00000248633.4:n.357+6G=
ENST00000248633.8:c.357+6G=	ENSP00000248633.4:n.357+6G=
ENST00000428214.5:c.357+6G=	ENSP00000394413.1:n.357+6G=
ENST00000438045.5:c.273+3113G=	ENSP00000410438.1:n.273+3113G=
ENST00000484913.5:n.367G=
NM_000466.2:c.357+6G=	NP_000457.1:n.357+6G=
NM_001282677.1:c.357+6G=	NP_001269606.1:n.357+6G=
NM_001282678.1:c.-297G=	NP_001269607.1:n.-297G=
XR_242246.3:n.453+6G=
XR_242246.5:n.404+6G=
NM_000466.3:c.357+6G= MANE Select	NP_000457.1:n.357+6G=
NM_001282677.2:c.357+6G=	NP_001269606.1:n.357+6G=
NM_001282678.2:c.-297G=	NP_001269607.1:n.-297G=