Canonical Allele Identifier: CA1725935294

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92500026C= , CM000669.2:g.92500026C=	GRCh38
NC_000007.13:g.92129340C= , CM000669.1:g.92129340C=	GRCh37
NC_000007.12:g.91967276C=	NCBI36
NG_008341.1:g.33506G=
NG_008341.2:g.33506G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2584-188G= MANE Select	ENSP00000248633.4:n.2584-188G=
ENST00000248633.8:c.2584-188G=	ENSP00000248633.4:n.2584-188G=
ENST00000428214.5:c.2413-188G=	ENSP00000394413.1:n.2413-188G=
ENST00000438045.5:c.1618-188G=	ENSP00000410438.1:n.1618-188G=
ENST00000484913.5:n.2623-188G=
ENST00000496420.5:n.2476-188G=
NM_000466.2:c.2584-188G=	NP_000457.1:n.2584-188G=
NM_001282677.1:c.2413-188G=	NP_001269606.1:n.2413-188G=
NM_001282678.1:c.1960-188G=	NP_001269607.1:n.1960-188G=
XM_005250433.3:c.835-188G=	XP_005250490.1:n.835-188G=
XR_242246.3:n.2680-188G=
XM_017012319.2:c.835-188G=	XP_016867808.1:n.835-188G=
XR_001744808.2:n.1611-188G=
XR_242246.5:n.2631-188G=
NM_000466.3:c.2584-188G= MANE Select	NP_000457.1:n.2584-188G=
NM_001282677.2:c.2413-188G=	NP_001269606.1:n.2413-188G=
NM_001282678.2:c.1960-188G=	NP_001269607.1:n.1960-188G=