Canonical Allele Identifier: CA368174132

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92129127G>T (hg19) ; chr7:g.92499813G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499813G>T , CM000669.2:g.92499813G>T	GRCh38
NC_000007.13:g.92129127G>T , CM000669.1:g.92129127G>T	GRCh37
NC_000007.12:g.91967063G>T	NCBI36
NG_008341.1:g.33719C>A
NG_008341.2:g.33719C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2609C>A MANE Select	ENSP00000248633.4:p.Pro870His
ENST00000248633.8:c.2609C>A	ENSP00000248633.4:p.Pro870His
ENST00000428214.5:c.2438C>A	ENSP00000394413.1:p.Pro813His
ENST00000438045.5:c.1643C>A	ENSP00000410438.1:p.Pro548His
ENST00000484913.5:n.2648C>A
ENST00000496420.5:n.2501C>A
NM_000466.2:c.2609C>A	NP_000457.1:p.Pro870His
NM_001282677.1:c.2438C>A	NP_001269606.1:p.Pro813His
NM_001282678.1:c.1985C>A	NP_001269607.1:p.Pro662His
XM_005250433.3:c.860C>A	XP_005250490.1:p.Pro287His
XR_242246.3:n.2705C>A
XM_017012319.2:c.860C>A	XP_016867808.1:p.Pro287His
XR_001744808.2:n.1636C>A
XR_242246.5:n.2656C>A
NM_000466.3:c.2609C>A MANE Select	NP_000457.1:p.Pro870His
NM_001282677.2:c.2438C>A	NP_001269606.1:p.Pro813His
NM_001282678.2:c.1985C>A	NP_001269607.1:p.Pro662His