Canonical Allele Identifier: CA456482994

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92131376A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92502062A>T , CM000669.2:g.92502062A>T	GRCh38
NC_000007.13:g.92131376A>T , CM000669.1:g.92131376A>T	GRCh37
NC_000007.12:g.91969312A>T	NCBI36
NG_008341.1:g.31470T>A
NG_008341.2:g.31470T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2244T>A MANE Select	ENSP00000248633.4:p.Ile748=
ENST00000248633.8:c.2244T>A	ENSP00000248633.4:p.Ile748=
ENST00000428214.5:c.2073T>A	ENSP00000394413.1:p.Ile691=
ENST00000438045.5:c.1278T>A	ENSP00000410438.1:p.Ile426=
ENST00000484913.5:n.2283T>A
ENST00000496092.1:n.42T>A
ENST00000496420.5:n.1920T>A
NM_000466.2:c.2244T>A	NP_000457.1:p.Ile748=
NM_001282677.1:c.2073T>A	NP_001269606.1:p.Ile691=
NM_001282678.1:c.1620T>A	NP_001269607.1:p.Ile540=
XM_005250433.3:c.495T>A	XP_005250490.1:p.Ile165=
XR_242246.3:n.2340T>A
XM_017012319.2:c.495T>A	XP_016867808.1:p.Ile165=
XR_001744808.2:n.1271T>A
XR_242246.5:n.2291T>A
NM_000466.3:c.2244T>A MANE Select	NP_000457.1:p.Ile748=
NM_001282677.2:c.2073T>A	NP_001269606.1:p.Ile691=
NM_001282678.2:c.1620T>A	NP_001269607.1:p.Ile540=