Canonical Allele Identifier: CA368199813

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92147036A>T (hg19) ; chr7:g.92517722A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517722A>T , CM000669.2:g.92517722A>T	GRCh38
NC_000007.13:g.92147036A>T , CM000669.1:g.92147036A>T	GRCh37
NC_000007.12:g.91984972A>T	NCBI36
NG_008341.1:g.15810T>A
NG_008341.2:g.15810T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.793T>A MANE Select	ENSP00000248633.4:p.Trp265Arg
ENST00000248633.8:c.793T>A	ENSP00000248633.4:p.Trp265Arg
ENST00000428214.5:c.793T>A	ENSP00000394413.1:p.Trp265Arg
ENST00000438045.5:c.274-3755T>A	ENSP00000410438.1:n.274-3755T>A
ENST00000484913.5:n.832T>A
NM_000466.2:c.793T>A	NP_000457.1:p.Trp265Arg
NM_001282677.1:c.793T>A	NP_001269606.1:p.Trp265Arg
NM_001282678.1:c.169T>A	NP_001269607.1:p.Trp57Arg
XR_242246.3:n.889T>A
XR_242246.5:n.840T>A
NM_000466.3:c.793T>A MANE Select	NP_000457.1:p.Trp265Arg
NM_001282677.2:c.793T>A	NP_001269606.1:p.Trp265Arg
NM_001282678.2:c.169T>A	NP_001269607.1:p.Trp57Arg