Canonical Allele Identifier: CA2683718656

Gene: PEX1

Linked Data

• gnomAD v4: 7-92504592-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504592T>A , CM000669.2:g.92504592T>A	GRCh38
NC_000007.13:g.92133906T>A , CM000669.1:g.92133906T>A	GRCh37
NC_000007.12:g.91971842T>A	NCBI36
NG_008341.1:g.28940A>T
NG_008341.2:g.28940A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2071+140A>T MANE Select	ENSP00000248633.4:n.2071+140A>T
ENST00000248633.8:c.2071+140A>T	ENSP00000248633.4:n.2071+140A>T
ENST00000428214.5:c.1901-1397A>T	ENSP00000394413.1:n.1901-1397A>T
ENST00000438045.5:c.1105+140A>T	ENSP00000410438.1:n.1105+140A>T
ENST00000484913.5:n.2110+140A>T
ENST00000496420.5:n.1747+140A>T
NM_000466.2:c.2071+140A>T	NP_000457.1:n.2071+140A>T
NM_001282677.1:c.1901-1397A>T	NP_001269606.1:n.1901-1397A>T
NM_001282678.1:c.1447+140A>T	NP_001269607.1:n.1447+140A>T
XM_005250433.3:c.322+140A>T	XP_005250490.1:n.322+140A>T
XR_242246.3:n.2167+140A>T
XM_017012319.2:c.322+140A>T	XP_016867808.1:n.322+140A>T
XR_001744808.2:n.1098+140A>T
XR_242246.5:n.2118+140A>T
NM_000466.3:c.2071+140A>T MANE Select	NP_000457.1:n.2071+140A>T
NM_001282677.2:c.1901-1397A>T	NP_001269606.1:n.1901-1397A>T
NM_001282678.2:c.1447+140A>T	NP_001269607.1:n.1447+140A>T