Canonical Allele Identifier: CA456624402

Gene: PEX1

Linked Data

• dbSNP Id: rs1362124917
• gnomAD v2: 7-92146914-A-C
• gnomAD v4: 7-92517600-A-C
• MyVariant Identifiers: chr7:g.92146914A>C (hg19) ; chr7:g.92517600A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517600A>C , CM000669.2:g.92517600A>C	GRCh38
NC_000007.13:g.92146914A>C , CM000669.1:g.92146914A>C	GRCh37
NC_000007.12:g.91984850A>C	NCBI36
NG_008341.1:g.15932T>G
NG_008341.2:g.15932T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.915T>G MANE Select	ENSP00000248633.4:p.Val305=
ENST00000248633.8:c.915T>G	ENSP00000248633.4:p.Val305=
ENST00000428214.5:c.915T>G	ENSP00000394413.1:p.Val305=
ENST00000438045.5:c.274-3633T>G	ENSP00000410438.1:n.274-3633T>G
ENST00000484913.5:n.954T>G
NM_000466.2:c.915T>G	NP_000457.1:p.Val305=
NM_001282677.1:c.915T>G	NP_001269606.1:p.Val305=
NM_001282678.1:c.291T>G	NP_001269607.1:p.Val97=
XR_242246.3:n.1011T>G
XM_017012319.2:c.-752T>G	XP_016867808.1:n.-752T>G
XR_001744808.2:n.25T>G
XR_242246.5:n.962T>G
NM_000466.3:c.915T>G MANE Select	NP_000457.1:p.Val305=
NM_001282677.2:c.915T>G	NP_001269606.1:p.Val305=
NM_001282678.2:c.291T>G	NP_001269607.1:p.Val97=