Canonical Allele Identifier: CA368198096

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92146732T>G (hg19) ; chr7:g.92517418T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517418T>G , CM000669.2:g.92517418T>G	GRCh38
NC_000007.13:g.92146732T>G , CM000669.1:g.92146732T>G	GRCh37
NC_000007.12:g.91984668T>G	NCBI36
NG_008341.1:g.16114A>C
NG_008341.2:g.16114A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1097A>C MANE Select	ENSP00000248633.4:p.Asp366Ala
ENST00000248633.8:c.1097A>C	ENSP00000248633.4:p.Asp366Ala
ENST00000428214.5:c.1097A>C	ENSP00000394413.1:p.Asp366Ala
ENST00000438045.5:c.274-3451A>C	ENSP00000410438.1:n.274-3451A>C
ENST00000484913.5:n.1136A>C
NM_000466.2:c.1097A>C	NP_000457.1:p.Asp366Ala
NM_001282677.1:c.1097A>C	NP_001269606.1:p.Asp366Ala
NM_001282678.1:c.473A>C	NP_001269607.1:p.Asp158Ala
XR_242246.3:n.1193A>C
XM_017012319.2:c.-570A>C	XP_016867808.1:n.-570A>C
XR_001744808.2:n.207A>C
XR_242246.5:n.1144A>C
NM_000466.3:c.1097A>C MANE Select	NP_000457.1:p.Asp366Ala
NM_001282677.2:c.1097A>C	NP_001269606.1:p.Asp366Ala
NM_001282678.2:c.473A>C	NP_001269607.1:p.Asp158Ala