Canonical Allele Identifier: CA368202099

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92147476T>A (hg19) ; chr7:g.92518162T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518162T>A , CM000669.2:g.92518162T>A	GRCh38
NC_000007.13:g.92147476T>A , CM000669.1:g.92147476T>A	GRCh37
NC_000007.12:g.91985412T>A	NCBI36
NG_008341.1:g.15370A>T
NG_008341.2:g.15370A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.451A>T MANE Select	ENSP00000248633.4:p.Thr151Ser
ENST00000248633.8:c.451A>T	ENSP00000248633.4:p.Thr151Ser
ENST00000428214.5:c.451A>T	ENSP00000394413.1:p.Thr151Ser
ENST00000438045.5:c.273+3940A>T	ENSP00000410438.1:n.273+3940A>T
ENST00000484913.5:n.490A>T
NM_000466.2:c.451A>T	NP_000457.1:p.Thr151Ser
NM_001282677.1:c.451A>T	NP_001269606.1:p.Thr151Ser
NM_001282678.1:c.-174A>T	NP_001269607.1:n.-174A>T
XR_242246.3:n.547A>T
XR_242246.5:n.498A>T
NM_000466.3:c.451A>T MANE Select	NP_000457.1:p.Thr151Ser
NM_001282677.2:c.451A>T	NP_001269606.1:p.Thr151Ser
NM_001282678.2:c.-174A>T	NP_001269607.1:n.-174A>T