Canonical Allele Identifier: CA368182289

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92132503T>G (hg19) ; chr7:g.92503189T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92503189T>G , CM000669.2:g.92503189T>G	GRCh38
NC_000007.13:g.92132503T>G , CM000669.1:g.92132503T>G	GRCh37
NC_000007.12:g.91970439T>G	NCBI36
NG_008341.1:g.30343A>C
NG_008341.2:g.30343A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2078A>C MANE Select	ENSP00000248633.4:p.Asn693Thr
ENST00000248633.8:c.2078A>C	ENSP00000248633.4:p.Asn693Thr
ENST00000428214.5:c.1907A>C	ENSP00000394413.1:p.Asn636Thr
ENST00000438045.5:c.1112A>C	ENSP00000410438.1:p.Asn371Thr
ENST00000484913.5:n.2117A>C
ENST00000496420.5:n.1754A>C
NM_000466.2:c.2078A>C	NP_000457.1:p.Asn693Thr
NM_001282677.1:c.1907A>C	NP_001269606.1:p.Asn636Thr
NM_001282678.1:c.1454A>C	NP_001269607.1:p.Asn485Thr
XM_005250433.3:c.329A>C	XP_005250490.1:p.Asn110Thr
XR_242246.3:n.2174A>C
XM_017012319.2:c.329A>C	XP_016867808.1:p.Asn110Thr
XR_001744808.2:n.1105A>C
XR_242246.5:n.2125A>C
NM_000466.3:c.2078A>C MANE Select	NP_000457.1:p.Asn693Thr
NM_001282677.2:c.1907A>C	NP_001269606.1:p.Asn636Thr
NM_001282678.2:c.1454A>C	NP_001269607.1:p.Asn485Thr