Canonical Allele Identifier: CA576304216

Gene: PEX1

Linked Data

• dbSNP Id: rs1225953829
• gnomAD v2: 7-92128905-G-T
• gnomAD v3: 7-92499591-G-T
• gnomAD v4: 7-92499591-G-T
• MyVariant Identifiers: chr7:g.92128905G>T (hg19) ; chr7:g.92499591G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499591G>T , CM000669.2:g.92499591G>T	GRCh38
NC_000007.13:g.92128905G>T , CM000669.1:g.92128905G>T	GRCh37
NC_000007.12:g.91966841G>T	NCBI36
NG_008341.1:g.33941C>A
NG_008341.2:g.33941C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2718+113C>A MANE Select	ENSP00000248633.4:n.2718+113C>A
ENST00000248633.8:c.2718+113C>A	ENSP00000248633.4:n.2718+113C>A
ENST00000428214.5:c.2547+113C>A	ENSP00000394413.1:n.2547+113C>A
ENST00000438045.5:c.1752+113C>A	ENSP00000410438.1:n.1752+113C>A
ENST00000484913.5:n.2757+113C>A
ENST00000496420.5:n.2610+113C>A
NM_000466.2:c.2718+113C>A	NP_000457.1:n.2718+113C>A
NM_001282677.1:c.2547+113C>A	NP_001269606.1:n.2547+113C>A
NM_001282678.1:c.2094+113C>A	NP_001269607.1:n.2094+113C>A
XM_005250433.3:c.969+113C>A	XP_005250490.1:n.969+113C>A
XR_242246.3:n.2814+113C>A
XM_017012319.2:c.969+113C>A	XP_016867808.1:n.969+113C>A
XR_001744808.2:n.1745+113C>A
XR_242246.5:n.2765+113C>A
NM_000466.3:c.2718+113C>A MANE Select	NP_000457.1:n.2718+113C>A
NM_001282677.2:c.2547+113C>A	NP_001269606.1:n.2547+113C>A
NM_001282678.2:c.2094+113C>A	NP_001269607.1:n.2094+113C>A