Canonical Allele Identifier: CA368200342

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92147116T>G (hg19) ; chr7:g.92517802T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517802T>G , CM000669.2:g.92517802T>G	GRCh38
NC_000007.13:g.92147116T>G , CM000669.1:g.92147116T>G	GRCh37
NC_000007.12:g.91985052T>G	NCBI36
NG_008341.1:g.15730A>C
NG_008341.2:g.15730A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.713A>C MANE Select	ENSP00000248633.4:p.Asp238Ala
ENST00000248633.8:c.713A>C	ENSP00000248633.4:p.Asp238Ala
ENST00000428214.5:c.713A>C	ENSP00000394413.1:p.Asp238Ala
ENST00000438045.5:c.274-3835A>C	ENSP00000410438.1:n.274-3835A>C
ENST00000484913.5:n.752A>C
NM_000466.2:c.713A>C	NP_000457.1:p.Asp238Ala
NM_001282677.1:c.713A>C	NP_001269606.1:p.Asp238Ala
NM_001282678.1:c.89A>C	NP_001269607.1:p.Asp30Ala
XR_242246.3:n.809A>C
XR_242246.5:n.760A>C
NM_000466.3:c.713A>C MANE Select	NP_000457.1:p.Asp238Ala
NM_001282677.2:c.713A>C	NP_001269606.1:p.Asp238Ala
NM_001282678.2:c.89A>C	NP_001269607.1:p.Asp30Ala