Canonical Allele Identifier: CA368198742

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92146862C>A (hg19) ; chr7:g.92517548C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517548C>A , CM000669.2:g.92517548C>A	GRCh38
NC_000007.13:g.92146862C>A , CM000669.1:g.92146862C>A	GRCh37
NC_000007.12:g.91984798C>A	NCBI36
NG_008341.1:g.15984G>T
NG_008341.2:g.15984G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.967G>T MANE Select	ENSP00000248633.4:p.Asp323Tyr
ENST00000248633.8:c.967G>T	ENSP00000248633.4:p.Asp323Tyr
ENST00000428214.5:c.967G>T	ENSP00000394413.1:p.Asp323Tyr
ENST00000438045.5:c.274-3581G>T	ENSP00000410438.1:n.274-3581G>T
ENST00000484913.5:n.1006G>T
NM_000466.2:c.967G>T	NP_000457.1:p.Asp323Tyr
NM_001282677.1:c.967G>T	NP_001269606.1:p.Asp323Tyr
NM_001282678.1:c.343G>T	NP_001269607.1:p.Asp115Tyr
XR_242246.3:n.1063G>T
XM_017012319.2:c.-700G>T	XP_016867808.1:n.-700G>T
XR_001744808.2:n.77G>T
XR_242246.5:n.1014G>T
NM_000466.3:c.967G>T MANE Select	NP_000457.1:p.Asp323Tyr
NM_001282677.2:c.967G>T	NP_001269606.1:p.Asp323Tyr
NM_001282678.2:c.343G>T	NP_001269607.1:p.Asp115Tyr