Canonical Allele Identifier: CA368176947

Gene: PEX1

Linked Data

• dbSNP Id: rs1287437057
• gnomAD v2: 7-92131213-T-C
• gnomAD v4: 7-92501899-T-C
• MyVariant Identifiers: chr7:g.92131213T>C (hg19) ; chr7:g.92501899T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92501899T>C , CM000669.2:g.92501899T>C	GRCh38
NC_000007.13:g.92131213T>C , CM000669.1:g.92131213T>C	GRCh37
NC_000007.12:g.91969149T>C	NCBI36
NG_008341.1:g.31633A>G
NG_008341.2:g.31633A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2407A>G MANE Select	ENSP00000248633.4:p.Thr803Ala
ENST00000248633.8:c.2407A>G	ENSP00000248633.4:p.Thr803Ala
ENST00000428214.5:c.2236A>G	ENSP00000394413.1:p.Thr746Ala
ENST00000438045.5:c.1441A>G	ENSP00000410438.1:p.Thr481Ala
ENST00000484913.5:n.2446A>G
ENST00000496092.1:n.205A>G
ENST00000496420.5:n.2083A>G
NM_000466.2:c.2407A>G	NP_000457.1:p.Thr803Ala
NM_001282677.1:c.2236A>G	NP_001269606.1:p.Thr746Ala
NM_001282678.1:c.1783A>G	NP_001269607.1:p.Thr595Ala
XM_005250433.3:c.658A>G	XP_005250490.1:p.Thr220Ala
XR_242246.3:n.2503A>G
XM_017012319.2:c.658A>G	XP_016867808.1:p.Thr220Ala
XR_001744808.2:n.1434A>G
XR_242246.5:n.2454A>G
NM_000466.3:c.2407A>G MANE Select	NP_000457.1:p.Thr803Ala
NM_001282677.2:c.2236A>G	NP_001269606.1:p.Thr746Ala
NM_001282678.2:c.1783A>G	NP_001269607.1:p.Thr595Ala