Canonical Allele Identifier: CA368178608

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92131368T>A (hg19) ; chr7:g.92502054T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92502054T>A , CM000669.2:g.92502054T>A	GRCh38
NC_000007.13:g.92131368T>A , CM000669.1:g.92131368T>A	GRCh37
NC_000007.12:g.91969304T>A	NCBI36
NG_008341.1:g.31478A>T
NG_008341.2:g.31478A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2252A>T MANE Select	ENSP00000248633.4:p.Asn751Ile
ENST00000248633.8:c.2252A>T	ENSP00000248633.4:p.Asn751Ile
ENST00000428214.5:c.2081A>T	ENSP00000394413.1:p.Asn694Ile
ENST00000438045.5:c.1286A>T	ENSP00000410438.1:p.Asn429Ile
ENST00000484913.5:n.2291A>T
ENST00000496092.1:n.50A>T
ENST00000496420.5:n.1928A>T
NM_000466.2:c.2252A>T	NP_000457.1:p.Asn751Ile
NM_001282677.1:c.2081A>T	NP_001269606.1:p.Asn694Ile
NM_001282678.1:c.1628A>T	NP_001269607.1:p.Asn543Ile
XM_005250433.3:c.503A>T	XP_005250490.1:p.Asn168Ile
XR_242246.3:n.2348A>T
XM_017012319.2:c.503A>T	XP_016867808.1:p.Asn168Ile
XR_001744808.2:n.1279A>T
XR_242246.5:n.2299A>T
NM_000466.3:c.2252A>T MANE Select	NP_000457.1:p.Asn751Ile
NM_001282677.2:c.2081A>T	NP_001269606.1:p.Asn694Ile
NM_001282678.2:c.1628A>T	NP_001269607.1:p.Asn543Ile