Canonical Allele Identifier: CA368202121

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92147479G>T (hg19) ; chr7:g.92518165G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518165G>T , CM000669.2:g.92518165G>T	GRCh38
NC_000007.13:g.92147479G>T , CM000669.1:g.92147479G>T	GRCh37
NC_000007.12:g.91985415G>T	NCBI36
NG_008341.1:g.15367C>A
NG_008341.2:g.15367C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.448C>A MANE Select	ENSP00000248633.4:p.Gln150Lys
ENST00000248633.8:c.448C>A	ENSP00000248633.4:p.Gln150Lys
ENST00000428214.5:c.448C>A	ENSP00000394413.1:p.Gln150Lys
ENST00000438045.5:c.273+3937C>A	ENSP00000410438.1:n.273+3937C>A
ENST00000484913.5:n.487C>A
NM_000466.2:c.448C>A	NP_000457.1:p.Gln150Lys
NM_001282677.1:c.448C>A	NP_001269606.1:p.Gln150Lys
NM_001282678.1:c.-177C>A	NP_001269607.1:n.-177C>A
XR_242246.3:n.544C>A
XR_242246.5:n.495C>A
NM_000466.3:c.448C>A MANE Select	NP_000457.1:p.Gln150Lys
NM_001282677.2:c.448C>A	NP_001269606.1:p.Gln150Lys
NM_001282678.2:c.-177C>A	NP_001269607.1:n.-177C>A