Canonical Allele Identifier: CA368181279

Gene: PEX1

Linked Data

• dbSNP Id: rs1281134878
• gnomAD v3: 7-92503070-A-C
• gnomAD v4: 7-92503070-A-C
• MyVariant Identifiers: chr7:g.92132384A>C (hg19) ; chr7:g.92503070A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92503070A>C , CM000669.2:g.92503070A>C	GRCh38
NC_000007.13:g.92132384A>C , CM000669.1:g.92132384A>C	GRCh37
NC_000007.12:g.91970320A>C	NCBI36
NG_008341.1:g.30462T>G
NG_008341.2:g.30462T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2197T>G MANE Select	ENSP00000248633.4:p.Cys733Gly
ENST00000248633.8:c.2197T>G	ENSP00000248633.4:p.Cys733Gly
ENST00000428214.5:c.2026T>G	ENSP00000394413.1:p.Cys676Gly
ENST00000438045.5:c.1231T>G	ENSP00000410438.1:p.Cys411Gly
ENST00000484913.5:n.2236T>G
ENST00000496420.5:n.1873T>G
NM_000466.2:c.2197T>G	NP_000457.1:p.Cys733Gly
NM_001282677.1:c.2026T>G	NP_001269606.1:p.Cys676Gly
NM_001282678.1:c.1573T>G	NP_001269607.1:p.Cys525Gly
XM_005250433.3:c.448T>G	XP_005250490.1:p.Cys150Gly
XR_242246.3:n.2293T>G
XM_017012319.2:c.448T>G	XP_016867808.1:p.Cys150Gly
XR_001744808.2:n.1224T>G
XR_242246.5:n.2244T>G
NM_000466.3:c.2197T>G MANE Select	NP_000457.1:p.Cys733Gly
NM_001282677.2:c.2026T>G	NP_001269606.1:p.Cys676Gly
NM_001282678.2:c.1573T>G	NP_001269607.1:p.Cys525Gly