Canonical Allele Identifier: CA368171151

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92126072T>A (hg19) ; chr7:g.92496758T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496758T>A , CM000669.2:g.92496758T>A	GRCh38
NC_000007.13:g.92126072T>A , CM000669.1:g.92126072T>A	GRCh37
NC_000007.12:g.91964008T>A	NCBI36
NG_008341.1:g.36774A>T
NG_008341.2:g.36774A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2738A>T MANE Select	ENSP00000248633.4:p.Lys913Ile
ENST00000248633.8:c.2738A>T	ENSP00000248633.4:p.Lys913Ile
ENST00000428214.5:c.2567A>T	ENSP00000394413.1:p.Lys856Ile
ENST00000438045.5:c.1772A>T	ENSP00000410438.1:p.Lys591Ile
ENST00000484913.5:n.2777A>T
ENST00000496420.5:n.2630A>T
NM_000466.2:c.2738A>T	NP_000457.1:p.Lys913Ile
NM_001282677.1:c.2567A>T	NP_001269606.1:p.Lys856Ile
NM_001282678.1:c.2114A>T	NP_001269607.1:p.Lys705Ile
XM_005250433.3:c.989A>T	XP_005250490.1:p.Lys330Ile
XR_242246.3:n.2834A>T
XM_017012319.2:c.989A>T	XP_016867808.1:p.Lys330Ile
XR_001744808.2:n.1765A>T
XR_242246.5:n.2785A>T
NM_000466.3:c.2738A>T MANE Select	NP_000457.1:p.Lys913Ile
NM_001282677.2:c.2567A>T	NP_001269606.1:p.Lys856Ile
NM_001282678.2:c.2114A>T	NP_001269607.1:p.Lys705Ile