Canonical Allele Identifier: CA456624363

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92146896G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517582G>C , CM000669.2:g.92517582G>C	GRCh38
NC_000007.13:g.92146896G>C , CM000669.1:g.92146896G>C	GRCh37
NC_000007.12:g.91984832G>C	NCBI36
NG_008341.1:g.15950C>G
NG_008341.2:g.15950C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.933C>G MANE Select	ENSP00000248633.4:p.Ala311=
ENST00000248633.8:c.933C>G	ENSP00000248633.4:p.Ala311=
ENST00000428214.5:c.933C>G	ENSP00000394413.1:p.Ala311=
ENST00000438045.5:c.274-3615C>G	ENSP00000410438.1:n.274-3615C>G
ENST00000484913.5:n.972C>G
NM_000466.2:c.933C>G	NP_000457.1:p.Ala311=
NM_001282677.1:c.933C>G	NP_001269606.1:p.Ala311=
NM_001282678.1:c.309C>G	NP_001269607.1:p.Ala103=
XR_242246.3:n.1029C>G
XM_017012319.2:c.-734C>G	XP_016867808.1:n.-734C>G
XR_001744808.2:n.43C>G
XR_242246.5:n.980C>G
NM_000466.3:c.933C>G MANE Select	NP_000457.1:p.Ala311=
NM_001282677.2:c.933C>G	NP_001269606.1:p.Ala311=
NM_001282678.2:c.309C>G	NP_001269607.1:p.Ala103=