Canonical Allele Identifier: CA456483741

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92140342C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92511028C>A , CM000669.2:g.92511028C>A	GRCh38
NC_000007.13:g.92140342C>A , CM000669.1:g.92140342C>A	GRCh37
NC_000007.12:g.91978278C>A	NCBI36
NG_008341.1:g.22504G>T
NG_008341.2:g.22504G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1503G>T MANE Select	ENSP00000248633.4:p.Leu501=
ENST00000248633.8:c.1503G>T	ENSP00000248633.4:p.Leu501=
ENST00000422866.1:c.404G>T
ENST00000428214.5:c.1503G>T	ENSP00000394413.1:p.Leu501=
ENST00000438045.5:c.537G>T	ENSP00000410438.1:p.Leu179=
ENST00000476923.1:n.264G>T
ENST00000484913.5:n.1542G>T
NM_000466.2:c.1503G>T	NP_000457.1:p.Leu501=
NM_001282677.1:c.1503G>T	NP_001269606.1:p.Leu501=
NM_001282678.1:c.879G>T	NP_001269607.1:p.Leu293=
XM_005250433.3:c.-164G>T	XP_005250490.1:n.-164G>T
XR_242246.3:n.1599G>T
XM_017012319.2:c.-164G>T	XP_016867808.1:n.-164G>T
XR_001744808.2:n.613G>T
XR_242246.5:n.1550G>T
NM_000466.3:c.1503G>T MANE Select	NP_000457.1:p.Leu501=
NM_001282677.2:c.1503G>T	NP_001269606.1:p.Leu501=
NM_001282678.2:c.879G>T	NP_001269607.1:p.Leu293=