Canonical Allele Identifier: CA1725936799

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92502902T= , CM000669.2:g.92502902T=	GRCh38
NC_000007.13:g.92132216T= , CM000669.1:g.92132216T=	GRCh37
NC_000007.12:g.91970152T=	NCBI36
NG_008341.1:g.30630A=
NG_008341.2:g.30630A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2226+139A= MANE Select	ENSP00000248633.4:n.2226+139A=
ENST00000248633.8:c.2226+139A=	ENSP00000248633.4:n.2226+139A=
ENST00000428214.5:c.2055+139A=	ENSP00000394413.1:n.2055+139A=
ENST00000438045.5:c.1260+139A=	ENSP00000410438.1:n.1260+139A=
ENST00000484913.5:n.2265+139A=
ENST00000496092.1:n.24+139A=
ENST00000496420.5:n.1902+139A=
NM_000466.2:c.2226+139A=	NP_000457.1:n.2226+139A=
NM_001282677.1:c.2055+139A=	NP_001269606.1:n.2055+139A=
NM_001282678.1:c.1602+139A=	NP_001269607.1:n.1602+139A=
XM_005250433.3:c.477+139A=	XP_005250490.1:n.477+139A=
XR_242246.3:n.2322+139A=
XM_017012319.2:c.477+139A=	XP_016867808.1:n.477+139A=
XR_001744808.2:n.1253+139A=
XR_242246.5:n.2273+139A=
NM_000466.3:c.2226+139A= MANE Select	NP_000457.1:n.2226+139A=
NM_001282677.2:c.2055+139A=	NP_001269606.1:n.2055+139A=
NM_001282678.2:c.1602+139A=	NP_001269607.1:n.1602+139A=