Canonical Allele Identifier: CA1725933259

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496679T= , CM000669.2:g.92496679T=	GRCh38
NC_000007.13:g.92125993T= , CM000669.1:g.92125993T=	GRCh37
NC_000007.12:g.91963929T=	NCBI36
NG_008341.1:g.36853A=
NG_008341.2:g.36853A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2783+34A= MANE Select	ENSP00000248633.4:n.2783+34A=
ENST00000248633.8:c.2783+34A=	ENSP00000248633.4:n.2783+34A=
ENST00000428214.5:c.2612+34A=	ENSP00000394413.1:n.2612+34A=
ENST00000438045.5:c.1817+34A=	ENSP00000410438.1:n.1817+34A=
ENST00000484913.5:n.2822+34A=
ENST00000496420.5:n.2675+34A=
NM_000466.2:c.2783+34A=	NP_000457.1:n.2783+34A=
NM_001282677.1:c.2612+34A=	NP_001269606.1:n.2612+34A=
NM_001282678.1:c.2159+34A=	NP_001269607.1:n.2159+34A=
XM_005250433.3:c.1034+34A=	XP_005250490.1:n.1034+34A=
XR_242246.3:n.2879+34A=
XM_017012319.2:c.1034+34A=	XP_016867808.1:n.1034+34A=
XR_001744808.2:n.1810+34A=
XR_242246.5:n.2830+34A=
NM_000466.3:c.2783+34A= MANE Select	NP_000457.1:n.2783+34A=
NM_001282677.2:c.2612+34A=	NP_001269606.1:n.2612+34A=
NM_001282678.2:c.2159+34A=	NP_001269607.1:n.2159+34A=