Canonical Allele Identifier: CA368184021

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92134183T>A (hg19) ; chr7:g.92504869T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504869T>A , CM000669.2:g.92504869T>A	GRCh38
NC_000007.13:g.92134183T>A , CM000669.1:g.92134183T>A	GRCh37
NC_000007.12:g.91972119T>A	NCBI36
NG_008341.1:g.28663A>T
NG_008341.2:g.28663A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1934A>T MANE Select	ENSP00000248633.4:p.Glu645Val
ENST00000248633.8:c.1934A>T	ENSP00000248633.4:p.Glu645Val
ENST00000428214.5:c.1900+1379A>T	ENSP00000394413.1:n.1900+1379A>T
ENST00000438045.5:c.968A>T	ENSP00000410438.1:p.Glu323Val
ENST00000484913.5:n.1973A>T
ENST00000496420.5:n.1610A>T
NM_000466.2:c.1934A>T	NP_000457.1:p.Glu645Val
NM_001282677.1:c.1900+1379A>T	NP_001269606.1:n.1900+1379A>T
NM_001282678.1:c.1310A>T	NP_001269607.1:p.Glu437Val
XM_005250433.3:c.185A>T	XP_005250490.1:p.Glu62Val
XR_242246.3:n.2030A>T
XM_017012319.2:c.185A>T	XP_016867808.1:p.Glu62Val
XR_001744808.2:n.961A>T
XR_242246.5:n.1981A>T
NM_000466.3:c.1934A>T MANE Select	NP_000457.1:p.Glu645Val
NM_001282677.2:c.1900+1379A>T	NP_001269606.1:n.1900+1379A>T
NM_001282678.2:c.1310A>T	NP_001269607.1:p.Glu437Val