Canonical Allele Identifier: CA456481980

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92129072G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499758G>C , CM000669.2:g.92499758G>C	GRCh38
NC_000007.13:g.92129072G>C , CM000669.1:g.92129072G>C	GRCh37
NC_000007.12:g.91967008G>C	NCBI36
NG_008341.1:g.33774C>G
NG_008341.2:g.33774C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2664C>G MANE Select	ENSP00000248633.4:p.Thr888=
ENST00000248633.8:c.2664C>G	ENSP00000248633.4:p.Thr888=
ENST00000428214.5:c.2493C>G	ENSP00000394413.1:p.Thr831=
ENST00000438045.5:c.1698C>G	ENSP00000410438.1:p.Thr566=
ENST00000484913.5:n.2703C>G
ENST00000496420.5:n.2556C>G
NM_000466.2:c.2664C>G	NP_000457.1:p.Thr888=
NM_001282677.1:c.2493C>G	NP_001269606.1:p.Thr831=
NM_001282678.1:c.2040C>G	NP_001269607.1:p.Thr680=
XM_005250433.3:c.915C>G	XP_005250490.1:p.Thr305=
XR_242246.3:n.2760C>G
XM_017012319.2:c.915C>G	XP_016867808.1:p.Thr305=
XR_001744808.2:n.1691C>G
XR_242246.5:n.2711C>G
NM_000466.3:c.2664C>G MANE Select	NP_000457.1:p.Thr888=
NM_001282677.2:c.2493C>G	NP_001269606.1:p.Thr831=
NM_001282678.2:c.2040C>G	NP_001269607.1:p.Thr680=