Canonical Allele Identifier: CA576308368

Gene: PEX1

Linked Data

• dbSNP Id: rs1283099438
• gnomAD v2: 7-92148399-A-C
• gnomAD v4: 7-92519085-A-C
• MyVariant Identifiers: chr7:g.92148399A>C (hg19) ; chr7:g.92519085A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92519085A>C , CM000669.2:g.92519085A>C	GRCh38
NC_000007.13:g.92148399A>C , CM000669.1:g.92148399A>C	GRCh37
NC_000007.12:g.91986335A>C	NCBI36
NG_008341.1:g.14447T>G
NG_008341.2:g.14447T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.274-7T>G MANE Select	ENSP00000248633.4:n.274-7T>G
ENST00000248633.8:c.274-7T>G	ENSP00000248633.4:n.274-7T>G
ENST00000428214.5:c.274-7T>G	ENSP00000394413.1:n.274-7T>G
ENST00000438045.5:c.273+3017T>G	ENSP00000410438.1:n.273+3017T>G
ENST00000484913.5:n.278-7T>G
NM_000466.2:c.274-7T>G	NP_000457.1:n.274-7T>G
NM_001282677.1:c.274-7T>G	NP_001269606.1:n.274-7T>G
NM_001282678.1:c.-386-7T>G	NP_001269607.1:n.-386-7T>G
XR_242246.3:n.370-7T>G
XR_242246.5:n.321-7T>G
NM_000466.3:c.274-7T>G MANE Select	NP_000457.1:n.274-7T>G
NM_001282677.2:c.274-7T>G	NP_001269606.1:n.274-7T>G
NM_001282678.2:c.-386-7T>G	NP_001269607.1:n.-386-7T>G