Canonical Allele Identifier: CA456482869

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92131205T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92501891T>C , CM000669.2:g.92501891T>C	GRCh38
NC_000007.13:g.92131205T>C , CM000669.1:g.92131205T>C	GRCh37
NC_000007.12:g.91969141T>C	NCBI36
NG_008341.1:g.31641A>G
NG_008341.2:g.31641A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2415A>G MANE Select	ENSP00000248633.4:p.Glu805=
ENST00000248633.8:c.2415A>G	ENSP00000248633.4:p.Glu805=
ENST00000428214.5:c.2244A>G	ENSP00000394413.1:p.Glu748=
ENST00000438045.5:c.1449A>G	ENSP00000410438.1:p.Glu483=
ENST00000484913.5:n.2454A>G
ENST00000496092.1:n.213A>G
ENST00000496420.5:n.2091A>G
NM_000466.2:c.2415A>G	NP_000457.1:p.Glu805=
NM_001282677.1:c.2244A>G	NP_001269606.1:p.Glu748=
NM_001282678.1:c.1791A>G	NP_001269607.1:p.Glu597=
XM_005250433.3:c.666A>G	XP_005250490.1:p.Glu222=
XR_242246.3:n.2511A>G
XM_017012319.2:c.666A>G	XP_016867808.1:p.Glu222=
XR_001744808.2:n.1442A>G
XR_242246.5:n.2462A>G
NM_000466.3:c.2415A>G MANE Select	NP_000457.1:p.Glu805=
NM_001282677.2:c.2244A>G	NP_001269606.1:p.Glu748=
NM_001282678.2:c.1791A>G	NP_001269607.1:p.Glu597=