Canonical Allele Identifier: CA1725939205

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504902C= , CM000669.2:g.92504902C=	GRCh38
NC_000007.13:g.92134216C= , CM000669.1:g.92134216C=	GRCh37
NC_000007.12:g.91972152C=	NCBI36
NG_008341.1:g.28630G=
NG_008341.2:g.28630G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1901G= MANE Select	ENSP00000248633.4:p.Gly634=
ENST00000248633.8:c.1901G=	ENSP00000248633.4:p.Gly634=
ENST00000422866.1:c.719G=
ENST00000428214.5:c.1900+1346G=	ENSP00000394413.1:n.1900+1346G=
ENST00000438045.5:c.935G=	ENSP00000410438.1:p.Gly312=
ENST00000484913.5:n.1940G=
ENST00000496420.5:n.1577G=
NM_000466.2:c.1901G=	NP_000457.1:p.Gly634=
NM_001282677.1:c.1900+1346G=	NP_001269606.1:n.1900+1346G=
NM_001282678.1:c.1277G=	NP_001269607.1:p.Gly426=
XM_005250433.3:c.152G=	XP_005250490.1:p.Gly51=
XR_242246.3:n.1997G=
XM_017012319.2:c.152G=	XP_016867808.1:p.Gly51=
XR_001744808.2:n.928G=
XR_242246.5:n.1948G=
NM_000466.3:c.1901G= MANE Select	NP_000457.1:p.Gly634=
NM_001282677.2:c.1900+1346G=	NP_001269606.1:n.1900+1346G=
NM_001282678.2:c.1277G=	NP_001269607.1:p.Gly426=