Canonical Allele Identifier: CA368183412

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92134115C>T (hg19) ; chr7:g.92504801C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504801C>T , CM000669.2:g.92504801C>T	GRCh38
NC_000007.13:g.92134115C>T , CM000669.1:g.92134115C>T	GRCh37
NC_000007.12:g.91972051C>T	NCBI36
NG_008341.1:g.28731G>A
NG_008341.2:g.28731G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2002G>A MANE Select	ENSP00000248633.4:p.Ala668Thr
ENST00000248633.8:c.2002G>A	ENSP00000248633.4:p.Ala668Thr
ENST00000428214.5:c.1900+1447G>A	ENSP00000394413.1:n.1900+1447G>A
ENST00000438045.5:c.1036G>A	ENSP00000410438.1:p.Ala346Thr
ENST00000484913.5:n.2041G>A
ENST00000496420.5:n.1678G>A
NM_000466.2:c.2002G>A	NP_000457.1:p.Ala668Thr
NM_001282677.1:c.1900+1447G>A	NP_001269606.1:n.1900+1447G>A
NM_001282678.1:c.1378G>A	NP_001269607.1:p.Ala460Thr
XM_005250433.3:c.253G>A	XP_005250490.1:p.Ala85Thr
XR_242246.3:n.2098G>A
XM_017012319.2:c.253G>A	XP_016867808.1:p.Ala85Thr
XR_001744808.2:n.1029G>A
XR_242246.5:n.2049G>A
NM_000466.3:c.2002G>A MANE Select	NP_000457.1:p.Ala668Thr
NM_001282677.2:c.1900+1447G>A	NP_001269606.1:n.1900+1447G>A
NM_001282678.2:c.1378G>A	NP_001269607.1:p.Ala460Thr