Canonical Allele Identifier: CA4341037

Gene: PEX1

Linked Data

• ClinVar Variation Id: 1553940
• ClinVar RCV Id: RCV002189929
• dbSNP Id: rs772778880
• ExAC: 7:92126109 A / G
• gnomAD v2: 7-92126109-A-G
• gnomAD v3: 7-92496795-A-G
• gnomAD v4: 7-92496795-A-G
• MyVariant Identifiers: chr7:g.92126109A>G (hg19) ; chr7:g.92496795A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496795A>G , CM000669.2:g.92496795A>G	GRCh38
NC_000007.13:g.92126109A>G , CM000669.1:g.92126109A>G	GRCh37
NC_000007.12:g.91964045A>G	NCBI36
NG_008341.1:g.36737T>C
NG_008341.2:g.36737T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2719-18T>C MANE Select	ENSP00000248633.4:n.2719-18T>C
ENST00000248633.8:c.2719-18T>C	ENSP00000248633.4:n.2719-18T>C
ENST00000428214.5:c.2548-18T>C	ENSP00000394413.1:n.2548-18T>C
ENST00000438045.5:c.1753-18T>C	ENSP00000410438.1:n.1753-18T>C
ENST00000484913.5:n.2758-18T>C
ENST00000496420.5:n.2611-18T>C
NM_000466.2:c.2719-18T>C	NP_000457.1:n.2719-18T>C
NM_001282677.1:c.2548-18T>C	NP_001269606.1:n.2548-18T>C
NM_001282678.1:c.2095-18T>C	NP_001269607.1:n.2095-18T>C
XM_005250433.3:c.970-18T>C	XP_005250490.1:n.970-18T>C
XR_242246.3:n.2815-18T>C
XM_017012319.2:c.970-18T>C	XP_016867808.1:n.970-18T>C
XR_001744808.2:n.1746-18T>C
XR_242246.5:n.2766-18T>C
NM_000466.3:c.2719-18T>C MANE Select	NP_000457.1:n.2719-18T>C
NM_001282677.2:c.2548-18T>C	NP_001269606.1:n.2548-18T>C
NM_001282678.2:c.2095-18T>C	NP_001269607.1:n.2095-18T>C