Canonical Allele Identifier: CA368183415

Gene: PEX1

Linked Data

• gnomAD v4: 7-92504802-A-C
• MyVariant Identifiers: chr7:g.92134116A>C (hg19) ; chr7:g.92504802A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504802A>C , CM000669.2:g.92504802A>C	GRCh38
NC_000007.13:g.92134116A>C , CM000669.1:g.92134116A>C	GRCh37
NC_000007.12:g.91972052A>C	NCBI36
NG_008341.1:g.28730T>G
NG_008341.2:g.28730T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2001T>G MANE Select	ENSP00000248633.4:p.Ile667Met
ENST00000248633.8:c.2001T>G	ENSP00000248633.4:p.Ile667Met
ENST00000428214.5:c.1900+1446T>G	ENSP00000394413.1:n.1900+1446T>G
ENST00000438045.5:c.1035T>G	ENSP00000410438.1:p.Ile345Met
ENST00000484913.5:n.2040T>G
ENST00000496420.5:n.1677T>G
NM_000466.2:c.2001T>G	NP_000457.1:p.Ile667Met
NM_001282677.1:c.1900+1446T>G	NP_001269606.1:n.1900+1446T>G
NM_001282678.1:c.1377T>G	NP_001269607.1:p.Ile459Met
XM_005250433.3:c.252T>G	XP_005250490.1:p.Ile84Met
XR_242246.3:n.2097T>G
XM_017012319.2:c.252T>G	XP_016867808.1:p.Ile84Met
XR_001744808.2:n.1028T>G
XR_242246.5:n.2048T>G
NM_000466.3:c.2001T>G MANE Select	NP_000457.1:p.Ile667Met
NM_001282677.2:c.1900+1446T>G	NP_001269606.1:n.1900+1446T>G
NM_001282678.2:c.1377T>G	NP_001269607.1:p.Ile459Met