Canonical Allele Identifier: CA368174029

Gene: PEX1

Linked Data

• gnomAD v4: 7-92499801-C-T
• MyVariant Identifiers: chr7:g.92129115C>T (hg19) ; chr7:g.92499801C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499801C>T , CM000669.2:g.92499801C>T	GRCh38
NC_000007.13:g.92129115C>T , CM000669.1:g.92129115C>T	GRCh37
NC_000007.12:g.91967051C>T	NCBI36
NG_008341.1:g.33731G>A
NG_008341.2:g.33731G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2621G>A MANE Select	ENSP00000248633.4:p.Arg874Lys
ENST00000248633.8:c.2621G>A	ENSP00000248633.4:p.Arg874Lys
ENST00000428214.5:c.2450G>A	ENSP00000394413.1:p.Arg817Lys
ENST00000438045.5:c.1655G>A	ENSP00000410438.1:p.Arg552Lys
ENST00000484913.5:n.2660G>A
ENST00000496420.5:n.2513G>A
NM_000466.2:c.2621G>A	NP_000457.1:p.Arg874Lys
NM_001282677.1:c.2450G>A	NP_001269606.1:p.Arg817Lys
NM_001282678.1:c.1997G>A	NP_001269607.1:p.Arg666Lys
XM_005250433.3:c.872G>A	XP_005250490.1:p.Arg291Lys
XR_242246.3:n.2717G>A
XM_017012319.2:c.872G>A	XP_016867808.1:p.Arg291Lys
XR_001744808.2:n.1648G>A
XR_242246.5:n.2668G>A
NM_000466.3:c.2621G>A MANE Select	NP_000457.1:p.Arg874Lys
NM_001282677.2:c.2450G>A	NP_001269606.1:p.Arg817Lys
NM_001282678.2:c.1997G>A	NP_001269607.1:p.Arg666Lys