Canonical Allele Identifier: CA368184529

Gene: PEX1

Linked Data

• gnomAD v4: 7-92506248-C-T
• MyVariant Identifiers: chr7:g.92135562C>T (hg19) ; chr7:g.92506248C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506248C>T , CM000669.2:g.92506248C>T	GRCh38
NC_000007.13:g.92135562C>T , CM000669.1:g.92135562C>T	GRCh37
NC_000007.12:g.91973498C>T	NCBI36
NG_008341.1:g.27284G>A
NG_008341.2:g.27284G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1900G>A MANE Select	ENSP00000248633.4:p.Gly634Arg
ENST00000248633.8:c.1900G>A	ENSP00000248633.4:p.Gly634Arg
ENST00000422866.1:c.718G>A
ENST00000428214.5:c.1900G>A	ENSP00000394413.1:p.Ala634Thr
ENST00000438045.5:c.934G>A	ENSP00000410438.1:p.Gly312Arg
ENST00000484913.5:n.1939G>A
ENST00000496420.5:n.1576G>A
NM_000466.2:c.1900G>A	NP_000457.1:p.Gly634Arg
NM_001282677.1:c.1900G>A	NP_001269606.1:p.Ala634Thr
NM_001282678.1:c.1276G>A	NP_001269607.1:p.Gly426Arg
XM_005250433.3:c.151G>A	XP_005250490.1:p.Gly51Arg
XR_242246.3:n.1996G>A
XM_017012319.2:c.151G>A	XP_016867808.1:p.Gly51Arg
XR_001744808.2:n.927G>A
XR_242246.5:n.1947G>A
NM_000466.3:c.1900G>A MANE Select	NP_000457.1:p.Gly634Arg
NM_001282677.2:c.1900G>A	NP_001269606.1:p.Ala634Thr
NM_001282678.2:c.1276G>A	NP_001269607.1:p.Gly426Arg