Canonical Allele Identifier: CA368198660

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92146843G>T (hg19) ; chr7:g.92517529G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517529G>T , CM000669.2:g.92517529G>T	GRCh38
NC_000007.13:g.92146843G>T , CM000669.1:g.92146843G>T	GRCh37
NC_000007.12:g.91984779G>T	NCBI36
NG_008341.1:g.16003C>A
NG_008341.2:g.16003C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.986C>A MANE Select	ENSP00000248633.4:p.Thr329Asn
ENST00000248633.8:c.986C>A	ENSP00000248633.4:p.Thr329Asn
ENST00000428214.5:c.986C>A	ENSP00000394413.1:p.Thr329Asn
ENST00000438045.5:c.274-3562C>A	ENSP00000410438.1:n.274-3562C>A
ENST00000484913.5:n.1025C>A
NM_000466.2:c.986C>A	NP_000457.1:p.Thr329Asn
NM_001282677.1:c.986C>A	NP_001269606.1:p.Thr329Asn
NM_001282678.1:c.362C>A	NP_001269607.1:p.Thr121Asn
XR_242246.3:n.1082C>A
XM_017012319.2:c.-681C>A	XP_016867808.1:n.-681C>A
XR_001744808.2:n.96C>A
XR_242246.5:n.1033C>A
NM_000466.3:c.986C>A MANE Select	NP_000457.1:p.Thr329Asn
NM_001282677.2:c.986C>A	NP_001269606.1:p.Thr329Asn
NM_001282678.2:c.362C>A	NP_001269607.1:p.Thr121Asn