Canonical Allele Identifier: CA456482876

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92131214G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92501900G>A , CM000669.2:g.92501900G>A	GRCh38
NC_000007.13:g.92131214G>A , CM000669.1:g.92131214G>A	GRCh37
NC_000007.12:g.91969150G>A	NCBI36
NG_008341.1:g.31632C>T
NG_008341.2:g.31632C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2406C>T MANE Select	ENSP00000248633.4:p.Ser802=
ENST00000248633.8:c.2406C>T	ENSP00000248633.4:p.Ser802=
ENST00000428214.5:c.2235C>T	ENSP00000394413.1:p.Ser745=
ENST00000438045.5:c.1440C>T	ENSP00000410438.1:p.Ser480=
ENST00000484913.5:n.2445C>T
ENST00000496092.1:n.204C>T
ENST00000496420.5:n.2082C>T
NM_000466.2:c.2406C>T	NP_000457.1:p.Ser802=
NM_001282677.1:c.2235C>T	NP_001269606.1:p.Ser745=
NM_001282678.1:c.1782C>T	NP_001269607.1:p.Ser594=
XM_005250433.3:c.657C>T	XP_005250490.1:p.Ser219=
XR_242246.3:n.2502C>T
XM_017012319.2:c.657C>T	XP_016867808.1:p.Ser219=
XR_001744808.2:n.1433C>T
XR_242246.5:n.2453C>T
NM_000466.3:c.2406C>T MANE Select	NP_000457.1:p.Ser802=
NM_001282677.2:c.2235C>T	NP_001269606.1:p.Ser745=
NM_001282678.2:c.1782C>T	NP_001269607.1:p.Ser594=