Canonical Allele Identifier: CA456624204

Gene: PEX1

Linked Data

• gnomAD v4: 7-92517512-G-A
• MyVariant Identifiers: chr7:g.92146826G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517512G>A , CM000669.2:g.92517512G>A	GRCh38
NC_000007.13:g.92146826G>A , CM000669.1:g.92146826G>A	GRCh37
NC_000007.12:g.91984762G>A	NCBI36
NG_008341.1:g.16020C>T
NG_008341.2:g.16020C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1003C>T MANE Select	ENSP00000248633.4:p.Leu335=
ENST00000248633.8:c.1003C>T	ENSP00000248633.4:p.Leu335=
ENST00000428214.5:c.1003C>T	ENSP00000394413.1:p.Leu335=
ENST00000438045.5:c.274-3545C>T	ENSP00000410438.1:n.274-3545C>T
ENST00000484913.5:n.1042C>T
NM_000466.2:c.1003C>T	NP_000457.1:p.Leu335=
NM_001282677.1:c.1003C>T	NP_001269606.1:p.Leu335=
NM_001282678.1:c.379C>T	NP_001269607.1:p.Leu127=
XR_242246.3:n.1099C>T
XM_017012319.2:c.-664C>T	XP_016867808.1:n.-664C>T
XR_001744808.2:n.113C>T
XR_242246.5:n.1050C>T
NM_000466.3:c.1003C>T MANE Select	NP_000457.1:p.Leu335=
NM_001282677.2:c.1003C>T	NP_001269606.1:p.Leu335=
NM_001282678.2:c.379C>T	NP_001269607.1:p.Leu127=