Canonical Allele Identifier: CA368168300

Gene: PEX1 GATAD1

Linked Data

• MyVariant Identifiers: chr7:g.92123822C>T (hg19) ; chr7:g.92494508C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92494508C>T , CM000669.2:g.92494508C>T	GRCh38
NC_000007.13:g.92123822C>T , CM000669.1:g.92123822C>T	GRCh37
NC_000007.12:g.91961758C>T	NCBI36
NG_008341.1:g.39024G>A
NG_008341.2:g.39024G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2905G>A (PEX1) MANE Select	ENSP00000248633.4:p.Asp969Asn
ENST00000248633.8:c.2905G>A (PEX1)	ENSP00000248633.4:p.Asp969Asn
ENST00000428214.5:c.2734G>A (PEX1)	ENSP00000394413.1:p.Asp912Asn
ENST00000438045.5:c.1939G>A (PEX1)	ENSP00000410438.1:p.Asp647Asn
ENST00000484913.5:n.2944G>A (PEX1)
ENST00000496420.5:n.2797G>A (PEX1)
NM_000466.2:c.2905G>A (PEX1)	NP_000457.1:p.Asp969Asn
NM_001282677.1:c.2734G>A (PEX1)	NP_001269606.1:p.Asp912Asn
NM_001282678.1:c.2281G>A (PEX1)	NP_001269607.1:p.Asp761Asn
XM_005250433.3:c.1156G>A (PEX1)	XP_005250490.1:p.Asp386Asn
XR_242246.3:n.3001G>A (PEX1)
XM_017012319.2:c.1156G>A (PEX1)	XP_016867808.1:p.Asp386Asn
XR_001744808.2:n.1932G>A (PEX1)
XR_001744843.2:n.5477C>T (GATAD1)
XR_242246.5:n.2952G>A (PEX1)
XR_927494.3:n.4328C>T (GATAD1)
XR_927503.3:n.4259C>T (GATAD1)
NM_000466.3:c.2905G>A (PEX1) MANE Select	NP_000457.1:p.Asp969Asn
NM_001282677.2:c.2734G>A (PEX1)	NP_001269606.1:p.Asp912Asn
NM_001282678.2:c.2281G>A (PEX1)	NP_001269607.1:p.Asp761Asn