Canonical Allele Identifier: CA4341545

Gene: PEX1

Linked Data

• ClinVar Variation Id: 1984675
• ClinVar RCV Id: RCV002756875
• dbSNP Id: rs773866601
• ExAC: 7:92147061 T / C
• gnomAD v2: 7-92147061-T-C
• gnomAD v4: 7-92517747-T-C
• MyVariant Identifiers: chr7:g.92147061T>C (hg19) ; chr7:g.92517747T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517747T>C , CM000669.2:g.92517747T>C	GRCh38
NC_000007.13:g.92147061T>C , CM000669.1:g.92147061T>C	GRCh37
NC_000007.12:g.91984997T>C	NCBI36
NG_008341.1:g.15785A>G
NG_008341.2:g.15785A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.768A>G MANE Select	ENSP00000248633.4:p.Gln256=
ENST00000248633.8:c.768A>G	ENSP00000248633.4:p.Gln256=
ENST00000428214.5:c.768A>G	ENSP00000394413.1:p.Gln256=
ENST00000438045.5:c.274-3780A>G	ENSP00000410438.1:n.274-3780A>G
ENST00000484913.5:n.807A>G
NM_000466.2:c.768A>G	NP_000457.1:p.Gln256=
NM_001282677.1:c.768A>G	NP_001269606.1:p.Gln256=
NM_001282678.1:c.144A>G	NP_001269607.1:p.Gln48=
XR_242246.3:n.864A>G
XR_242246.5:n.815A>G
NM_000466.3:c.768A>G MANE Select	NP_000457.1:p.Gln256=
NM_001282677.2:c.768A>G	NP_001269606.1:p.Gln256=
NM_001282678.2:c.144A>G	NP_001269607.1:p.Gln48=