Canonical Allele Identifier: CA456483479

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92135596G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506282G>T , CM000669.2:g.92506282G>T	GRCh38
NC_000007.13:g.92135596G>T , CM000669.1:g.92135596G>T	GRCh37
NC_000007.12:g.91973532G>T	NCBI36
NG_008341.1:g.27250C>A
NG_008341.2:g.27250C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1866C>A MANE Select	ENSP00000248633.4:p.Ala622=
ENST00000248633.8:c.1866C>A	ENSP00000248633.4:p.Ala622=
ENST00000422866.1:c.684C>A
ENST00000428214.5:c.1866C>A	ENSP00000394413.1:p.Ala622=
ENST00000438045.5:c.900C>A	ENSP00000410438.1:p.Ala300=
ENST00000484913.5:n.1905C>A
ENST00000496420.5:n.1542C>A
NM_000466.2:c.1866C>A	NP_000457.1:p.Ala622=
NM_001282677.1:c.1866C>A	NP_001269606.1:p.Ala622=
NM_001282678.1:c.1242C>A	NP_001269607.1:p.Ala414=
XM_005250433.3:c.117C>A	XP_005250490.1:p.Ala39=
XR_242246.3:n.1962C>A
XM_017012319.2:c.117C>A	XP_016867808.1:p.Ala39=
XR_001744808.2:n.893C>A
XR_242246.5:n.1913C>A
NM_000466.3:c.1866C>A MANE Select	NP_000457.1:p.Ala622=
NM_001282677.2:c.1866C>A	NP_001269606.1:p.Ala622=
NM_001282678.2:c.1242C>A	NP_001269607.1:p.Ala414=