Canonical Allele Identifier: CA368173059

Gene: PEX1

Linked Data

• gnomAD v4: 7-92499702-A-T
• MyVariant Identifiers: chr7:g.92129016A>T (hg19) ; chr7:g.92499702A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499702A>T , CM000669.2:g.92499702A>T	GRCh38
NC_000007.13:g.92129016A>T , CM000669.1:g.92129016A>T	GRCh37
NC_000007.12:g.91966952A>T	NCBI36
NG_008341.1:g.33830T>A
NG_008341.2:g.33830T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2718+2T>A MANE Select	ENSP00000248633.4:n.2718+2T>A
ENST00000248633.8:c.2718+2T>A	ENSP00000248633.4:n.2718+2T>A
ENST00000428214.5:c.2547+2T>A	ENSP00000394413.1:n.2547+2T>A
ENST00000438045.5:c.1752+2T>A	ENSP00000410438.1:n.1752+2T>A
ENST00000484913.5:n.2757+2T>A
ENST00000496420.5:n.2610+2T>A
NM_000466.2:c.2718+2T>A	NP_000457.1:n.2718+2T>A
NM_001282677.1:c.2547+2T>A	NP_001269606.1:n.2547+2T>A
NM_001282678.1:c.2094+2T>A	NP_001269607.1:n.2094+2T>A
XM_005250433.3:c.969+2T>A	XP_005250490.1:n.969+2T>A
XR_242246.3:n.2814+2T>A
XM_017012319.2:c.969+2T>A	XP_016867808.1:n.969+2T>A
XR_001744808.2:n.1745+2T>A
XR_242246.5:n.2765+2T>A
NM_000466.3:c.2718+2T>A MANE Select	NP_000457.1:n.2718+2T>A
NM_001282677.2:c.2547+2T>A	NP_001269606.1:n.2547+2T>A
NM_001282678.2:c.2094+2T>A	NP_001269607.1:n.2094+2T>A