Canonical Allele Identifier: CA2683718152

Gene: PEX1

Linked Data

• gnomAD v4: 7-92496815-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496815A>T , CM000669.2:g.92496815A>T	GRCh38
NC_000007.13:g.92126129A>T , CM000669.1:g.92126129A>T	GRCh37
NC_000007.12:g.91964065A>T	NCBI36
NG_008341.1:g.36717T>A
NG_008341.2:g.36717T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2719-38T>A MANE Select	ENSP00000248633.4:n.2719-38T>A
ENST00000248633.8:c.2719-38T>A	ENSP00000248633.4:n.2719-38T>A
ENST00000428214.5:c.2548-38T>A	ENSP00000394413.1:n.2548-38T>A
ENST00000438045.5:c.1753-38T>A	ENSP00000410438.1:n.1753-38T>A
ENST00000484913.5:n.2758-38T>A
ENST00000496420.5:n.2611-38T>A
NM_000466.2:c.2719-38T>A	NP_000457.1:n.2719-38T>A
NM_001282677.1:c.2548-38T>A	NP_001269606.1:n.2548-38T>A
NM_001282678.1:c.2095-38T>A	NP_001269607.1:n.2095-38T>A
XM_005250433.3:c.970-38T>A	XP_005250490.1:n.970-38T>A
XR_242246.3:n.2815-38T>A
XM_017012319.2:c.970-38T>A	XP_016867808.1:n.970-38T>A
XR_001744808.2:n.1746-38T>A
XR_242246.5:n.2766-38T>A
NM_000466.3:c.2719-38T>A MANE Select	NP_000457.1:n.2719-38T>A
NM_001282677.2:c.2548-38T>A	NP_001269606.1:n.2548-38T>A
NM_001282678.2:c.2095-38T>A	NP_001269607.1:n.2095-38T>A