Canonical Allele Identifier: CA368190286

Gene: PEX1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92511020A>T , CM000669.2:g.92511020A>T	GRCh38
NC_000007.13:g.92140334A>T , CM000669.1:g.92140334A>T	GRCh37
NC_000007.12:g.91978270A>T	NCBI36
NG_008341.1:g.22512T>A
NG_008341.2:g.22512T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1511T>A MANE Select	ENSP00000248633.4:p.Val504Asp
ENST00000248633.8:c.1511T>A	ENSP00000248633.4:p.Val504Asp
ENST00000422866.1:c.412T>A
ENST00000428214.5:c.1511T>A	ENSP00000394413.1:p.Val504Asp
ENST00000438045.5:c.545T>A	ENSP00000410438.1:p.Val182Asp
ENST00000476923.1:n.272T>A
ENST00000484913.5:n.1550T>A
NM_000466.2:c.1511T>A	NP_000457.1:p.Val504Asp
NM_001282677.1:c.1511T>A	NP_001269606.1:p.Val504Asp
NM_001282678.1:c.887T>A	NP_001269607.1:p.Val296Asp
XM_005250433.3:c.-156T>A	XP_005250490.1:n.-156T>A
XR_242246.3:n.1607T>A
XM_017012319.2:c.-156T>A	XP_016867808.1:n.-156T>A
XR_001744808.2:n.621T>A
XR_242246.5:n.1558T>A
NM_000466.3:c.1511T>A MANE Select	NP_000457.1:p.Val504Asp
NM_001282677.2:c.1511T>A	NP_001269606.1:p.Val504Asp
NM_001282678.2:c.887T>A	NP_001269607.1:p.Val296Asp