Canonical Allele Identifier: CA368199687

Gene: PEX1

Linked Data

• dbSNP Id: rs1177803945
• gnomAD v2: 7-92147016-A-T
• MyVariant Identifiers: chr7:g.92147016A>T (hg19) ; chr7:g.92517702A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517702A>T , CM000669.2:g.92517702A>T	GRCh38
NC_000007.13:g.92147016A>T , CM000669.1:g.92147016A>T	GRCh37
NC_000007.12:g.91984952A>T	NCBI36
NG_008341.1:g.15830T>A
NG_008341.2:g.15830T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.813T>A MANE Select	ENSP00000248633.4:p.Asn271Lys
ENST00000248633.8:c.813T>A	ENSP00000248633.4:p.Asn271Lys
ENST00000428214.5:c.813T>A	ENSP00000394413.1:p.Asn271Lys
ENST00000438045.5:c.274-3735T>A	ENSP00000410438.1:n.274-3735T>A
ENST00000484913.5:n.852T>A
NM_000466.2:c.813T>A	NP_000457.1:p.Asn271Lys
NM_001282677.1:c.813T>A	NP_001269606.1:p.Asn271Lys
NM_001282678.1:c.189T>A	NP_001269607.1:p.Asn63Lys
XR_242246.3:n.909T>A
XR_242246.5:n.860T>A
NM_000466.3:c.813T>A MANE Select	NP_000457.1:p.Asn271Lys
NM_001282677.2:c.813T>A	NP_001269606.1:p.Asn271Lys
NM_001282678.2:c.189T>A	NP_001269607.1:p.Asn63Lys