Canonical Allele Identifier: CA368187319

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92136348G>T (hg19) ; chr7:g.92507034G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92507034G>T , CM000669.2:g.92507034G>T	GRCh38
NC_000007.13:g.92136348G>T , CM000669.1:g.92136348G>T	GRCh37
NC_000007.12:g.91974284G>T	NCBI36
NG_008341.1:g.26498C>A
NG_008341.2:g.26498C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1763C>A MANE Select	ENSP00000248633.4:p.Ala588Glu
ENST00000248633.8:c.1763C>A	ENSP00000248633.4:p.Ala588Glu
ENST00000422866.1:c.581C>A
ENST00000428214.5:c.1763C>A	ENSP00000394413.1:p.Ala588Glu
ENST00000438045.5:c.797C>A	ENSP00000410438.1:p.Ala266Glu
ENST00000484913.5:n.1802C>A
ENST00000496420.5:n.790C>A
NM_000466.2:c.1763C>A	NP_000457.1:p.Ala588Glu
NM_001282677.1:c.1763C>A	NP_001269606.1:p.Ala588Glu
NM_001282678.1:c.1139C>A	NP_001269607.1:p.Ala380Glu
XM_005250433.3:c.14C>A	XP_005250490.1:p.Ala5Glu
XR_242246.3:n.1859C>A
XM_017012319.2:c.14C>A	XP_016867808.1:p.Ala5Glu
XR_001744808.2:n.790C>A
XR_242246.5:n.1810C>A
NM_000466.3:c.1763C>A MANE Select	NP_000457.1:p.Ala588Glu
NM_001282677.2:c.1763C>A	NP_001269606.1:p.Ala588Glu
NM_001282678.2:c.1139C>A	NP_001269607.1:p.Ala380Glu