Canonical Allele Identifier: CA368199756

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92147027T>C (hg19) ; chr7:g.92517713T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517713T>C , CM000669.2:g.92517713T>C	GRCh38
NC_000007.13:g.92147027T>C , CM000669.1:g.92147027T>C	GRCh37
NC_000007.12:g.91984963T>C	NCBI36
NG_008341.1:g.15819A>G
NG_008341.2:g.15819A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.802A>G MANE Select	ENSP00000248633.4:p.Thr268Ala
ENST00000248633.8:c.802A>G	ENSP00000248633.4:p.Thr268Ala
ENST00000428214.5:c.802A>G	ENSP00000394413.1:p.Thr268Ala
ENST00000438045.5:c.274-3746A>G	ENSP00000410438.1:n.274-3746A>G
ENST00000484913.5:n.841A>G
NM_000466.2:c.802A>G	NP_000457.1:p.Thr268Ala
NM_001282677.1:c.802A>G	NP_001269606.1:p.Thr268Ala
NM_001282678.1:c.178A>G	NP_001269607.1:p.Thr60Ala
XR_242246.3:n.898A>G
XR_242246.5:n.849A>G
NM_000466.3:c.802A>G MANE Select	NP_000457.1:p.Thr268Ala
NM_001282677.2:c.802A>G	NP_001269606.1:p.Thr268Ala
NM_001282678.2:c.178A>G	NP_001269607.1:p.Thr60Ala