Canonical Allele Identifier: CA1725933234

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496644C= , CM000669.2:g.92496644C=	GRCh38
NC_000007.13:g.92125958C= , CM000669.1:g.92125958C=	GRCh37
NC_000007.12:g.91963894C=	NCBI36
NG_008341.1:g.36888G=
NG_008341.2:g.36888G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2783+69G= MANE Select	ENSP00000248633.4:n.2783+69G=
ENST00000248633.8:c.2783+69G=	ENSP00000248633.4:n.2783+69G=
ENST00000428214.5:c.2612+69G=	ENSP00000394413.1:n.2612+69G=
ENST00000438045.5:c.1817+69G=	ENSP00000410438.1:n.1817+69G=
ENST00000484913.5:n.2822+69G=
ENST00000496420.5:n.2675+69G=
NM_000466.2:c.2783+69G=	NP_000457.1:n.2783+69G=
NM_001282677.1:c.2612+69G=	NP_001269606.1:n.2612+69G=
NM_001282678.1:c.2159+69G=	NP_001269607.1:n.2159+69G=
XM_005250433.3:c.1034+69G=	XP_005250490.1:n.1034+69G=
XR_242246.3:n.2879+69G=
XM_017012319.2:c.1034+69G=	XP_016867808.1:n.1034+69G=
XR_001744808.2:n.1810+69G=
XR_242246.5:n.2830+69G=
NM_000466.3:c.2783+69G= MANE Select	NP_000457.1:n.2783+69G=
NM_001282677.2:c.2612+69G=	NP_001269606.1:n.2612+69G=
NM_001282678.2:c.2159+69G=	NP_001269607.1:n.2159+69G=