Canonical Allele Identifier: CA368200535

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92147152G>A (hg19) ; chr7:g.92517838G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517838G>A , CM000669.2:g.92517838G>A	GRCh38
NC_000007.13:g.92147152G>A , CM000669.1:g.92147152G>A	GRCh37
NC_000007.12:g.91985088G>A	NCBI36
NG_008341.1:g.15694C>T
NG_008341.2:g.15694C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.677C>T MANE Select	ENSP00000248633.4:p.Thr226Ile
ENST00000248633.8:c.677C>T	ENSP00000248633.4:p.Thr226Ile
ENST00000428214.5:c.677C>T	ENSP00000394413.1:p.Thr226Ile
ENST00000438045.5:c.274-3871C>T	ENSP00000410438.1:n.274-3871C>T
ENST00000484913.5:n.716C>T
NM_000466.2:c.677C>T	NP_000457.1:p.Thr226Ile
NM_001282677.1:c.677C>T	NP_001269606.1:p.Thr226Ile
NM_001282678.1:c.53C>T	NP_001269607.1:p.Thr18Ile
XR_242246.3:n.773C>T
XR_242246.5:n.724C>T
NM_000466.3:c.677C>T MANE Select	NP_000457.1:p.Thr226Ile
NM_001282677.2:c.677C>T	NP_001269606.1:p.Thr226Ile
NM_001282678.2:c.53C>T	NP_001269607.1:p.Thr18Ile