Canonical Allele Identifier: CA368177835

Gene: PEX1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92501988G>T , CM000669.2:g.92501988G>T	GRCh38
NC_000007.13:g.92131302G>T , CM000669.1:g.92131302G>T	GRCh37
NC_000007.12:g.91969238G>T	NCBI36
NG_008341.1:g.31544C>A
NG_008341.2:g.31544C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2318C>A MANE Select	ENSP00000248633.4:p.Ala773Asp
ENST00000248633.8:c.2318C>A	ENSP00000248633.4:p.Ala773Asp
ENST00000428214.5:c.2147C>A	ENSP00000394413.1:p.Ala716Asp
ENST00000438045.5:c.1352C>A	ENSP00000410438.1:p.Ala451Asp
ENST00000484913.5:n.2357C>A
ENST00000496092.1:n.116C>A
ENST00000496420.5:n.1994C>A
NM_000466.2:c.2318C>A	NP_000457.1:p.Ala773Asp
NM_001282677.1:c.2147C>A	NP_001269606.1:p.Ala716Asp
NM_001282678.1:c.1694C>A	NP_001269607.1:p.Ala565Asp
XM_005250433.3:c.569C>A	XP_005250490.1:p.Ala190Asp
XR_242246.3:n.2414C>A
XM_017012319.2:c.569C>A	XP_016867808.1:p.Ala190Asp
XR_001744808.2:n.1345C>A
XR_242246.5:n.2365C>A
NM_000466.3:c.2318C>A MANE Select	NP_000457.1:p.Ala773Asp
NM_001282677.2:c.2147C>A	NP_001269606.1:p.Ala716Asp
NM_001282678.2:c.1694C>A	NP_001269607.1:p.Ala565Asp