Canonical Allele Identifier: CA456623998

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92146776A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517462A>G , CM000669.2:g.92517462A>G	GRCh38
NC_000007.13:g.92146776A>G , CM000669.1:g.92146776A>G	GRCh37
NC_000007.12:g.91984712A>G	NCBI36
NG_008341.1:g.16070T>C
NG_008341.2:g.16070T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1053T>C MANE Select	ENSP00000248633.4:p.Asn351=
ENST00000248633.8:c.1053T>C	ENSP00000248633.4:p.Asn351=
ENST00000428214.5:c.1053T>C	ENSP00000394413.1:p.Asn351=
ENST00000438045.5:c.274-3495T>C	ENSP00000410438.1:n.274-3495T>C
ENST00000484913.5:n.1092T>C
NM_000466.2:c.1053T>C	NP_000457.1:p.Asn351=
NM_001282677.1:c.1053T>C	NP_001269606.1:p.Asn351=
NM_001282678.1:c.429T>C	NP_001269607.1:p.Asn143=
XR_242246.3:n.1149T>C
XM_017012319.2:c.-614T>C	XP_016867808.1:n.-614T>C
XR_001744808.2:n.163T>C
XR_242246.5:n.1100T>C
NM_000466.3:c.1053T>C MANE Select	NP_000457.1:p.Asn351=
NM_001282677.2:c.1053T>C	NP_001269606.1:p.Asn351=
NM_001282678.2:c.429T>C	NP_001269607.1:p.Asn143=