Canonical Allele Identifier: CA368167785

Gene: PEX1 GATAD1

Linked Data

• MyVariant Identifiers: chr7:g.92123695G>T (hg19) ; chr7:g.92494381G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92494381G>T , CM000669.2:g.92494381G>T	GRCh38
NC_000007.13:g.92123695G>T , CM000669.1:g.92123695G>T	GRCh37
NC_000007.12:g.91961631G>T	NCBI36
NG_008341.1:g.39151C>A
NG_008341.2:g.39151C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2942C>A (PEX1) MANE Select	ENSP00000248633.4:p.Ala981Asp
ENST00000248633.8:c.2942C>A (PEX1)	ENSP00000248633.4:p.Ala981Asp
ENST00000428214.5:c.2771C>A (PEX1)	ENSP00000394413.1:p.Ala924Asp
ENST00000438045.5:c.1976C>A (PEX1)	ENSP00000410438.1:p.Ala659Asp
ENST00000484913.5:n.2981C>A (PEX1)
ENST00000496420.5:n.2834C>A (PEX1)
NM_000466.2:c.2942C>A (PEX1)	NP_000457.1:p.Ala981Asp
NM_001282677.1:c.2771C>A (PEX1)	NP_001269606.1:p.Ala924Asp
NM_001282678.1:c.2318C>A (PEX1)	NP_001269607.1:p.Ala773Asp
XM_005250433.3:c.1193C>A (PEX1)	XP_005250490.1:p.Ala398Asp
XR_242246.3:n.3038C>A (PEX1)
XM_017012319.2:c.1193C>A (PEX1)	XP_016867808.1:p.Ala398Asp
XR_001744808.2:n.1969C>A (PEX1)
XR_001744843.2:n.5350G>T (GATAD1)
XR_242246.5:n.2989C>A (PEX1)
XR_927494.3:n.4201G>T (GATAD1)
XR_927503.3:n.4132G>T (GATAD1)
NM_000466.3:c.2942C>A (PEX1) MANE Select	NP_000457.1:p.Ala981Asp
NM_001282677.2:c.2771C>A (PEX1)	NP_001269606.1:p.Ala924Asp
NM_001282678.2:c.2318C>A (PEX1)	NP_001269607.1:p.Ala773Asp