Canonical Allele Identifier: CA368183484

Gene: PEX1

Linked Data

• gnomAD v4: 7-92504809-T-G
• MyVariant Identifiers: chr7:g.92134123T>G (hg19) ; chr7:g.92504809T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504809T>G , CM000669.2:g.92504809T>G	GRCh38
NC_000007.13:g.92134123T>G , CM000669.1:g.92134123T>G	GRCh37
NC_000007.12:g.91972059T>G	NCBI36
NG_008341.1:g.28723A>C
NG_008341.2:g.28723A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1994A>C MANE Select	ENSP00000248633.4:p.Asp665Ala
ENST00000248633.8:c.1994A>C	ENSP00000248633.4:p.Asp665Ala
ENST00000428214.5:c.1900+1439A>C	ENSP00000394413.1:n.1900+1439A>C
ENST00000438045.5:c.1028A>C	ENSP00000410438.1:p.Asp343Ala
ENST00000484913.5:n.2033A>C
ENST00000496420.5:n.1670A>C
NM_000466.2:c.1994A>C	NP_000457.1:p.Asp665Ala
NM_001282677.1:c.1900+1439A>C	NP_001269606.1:n.1900+1439A>C
NM_001282678.1:c.1370A>C	NP_001269607.1:p.Asp457Ala
XM_005250433.3:c.245A>C	XP_005250490.1:p.Asp82Ala
XR_242246.3:n.2090A>C
XM_017012319.2:c.245A>C	XP_016867808.1:p.Asp82Ala
XR_001744808.2:n.1021A>C
XR_242246.5:n.2041A>C
NM_000466.3:c.1994A>C MANE Select	NP_000457.1:p.Asp665Ala
NM_001282677.2:c.1900+1439A>C	NP_001269606.1:n.1900+1439A>C
NM_001282678.2:c.1370A>C	NP_001269607.1:p.Asp457Ala