Canonical Allele Identifier: CA368205022

Gene: PEX1

Linked Data

• dbSNP Id: rs1390045766
• MyVariant Identifiers: chr7:g.92151501C>A (hg19) ; chr7:g.92522187C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92522187C>A , CM000669.2:g.92522187C>A	GRCh38
NC_000007.13:g.92151501C>A , CM000669.1:g.92151501C>A	GRCh37
NC_000007.12:g.91989437C>A	NCBI36
NG_008341.1:g.11345G>T
NG_008341.2:g.11345G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.188G>T MANE Select	ENSP00000248633.4:p.Gly63Val
ENST00000248633.8:c.188G>T	ENSP00000248633.4:p.Gly63Val
ENST00000428214.5:c.188G>T	ENSP00000394413.1:p.Gly63Val
ENST00000438045.5:c.188G>T	ENSP00000410438.1:p.Gly63Val
ENST00000484913.5:n.192G>T
NM_000466.2:c.188G>T	NP_000457.1:p.Gly63Val
NM_001282677.1:c.188G>T	NP_001269606.1:p.Gly63Val
NM_001282678.1:c.-472G>T	NP_001269607.1:n.-472G>T
XR_242246.3:n.284G>T
XR_242246.5:n.235G>T
NM_000466.3:c.188G>T MANE Select	NP_000457.1:p.Gly63Val
NM_001282677.2:c.188G>T	NP_001269606.1:p.Gly63Val
NM_001282678.2:c.-472G>T	NP_001269607.1:n.-472G>T